Latest US product recalls
Fresh from the four federal safety agencies. RapidRecall checks every one of these against its users’ purchases automatically. This page is the manual version.
- FDASep 3, 2026
Heinz Real - Vraie Mayonnaise, 12.5ml single serving packet, 500 packets per case, case code 57000 06672
KRAFT HEINZ FOODS COMPANY
undeclared ingredients including but not limited to mustard FDA Not Yet Classified recall.
- FDAAug 28, 2026
Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ingredients: haw, white sugar, water.; Serving suggestion: ready to eat. Storage: keep in cool and dry place and keep tightly closed in refrigerator after opening.; PRODUCT OF CHINA; UPC 6 920603 810025
Tiffany Food Corp
Unapproved dye Ponceau 4R FDA Class III recall.
- FDAAug 28, 2026
Organic Triple Berry Blend Strawberries, Blackberries & Blueberries, NET WT 10 OZ (283g), packed in plastic bag, 5 bags per case of 10 OZ each. KEEP FROZEN
Frutas y Hortalizas del Sur S.A.
Potential E. coli O145:H28 Contamination FDA Class I recall.
- FDAAug 26, 2026
Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8
FOODS ALIVE INC.
Potential Salmonella contamination FDA Class I recall.
- FDAAug 25, 2026
Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2 units each, Keep Refrigerated
Optimus Inc. d/b/a/ Markys Caviar
The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes. FDA Class I recall.
- FDAAug 25, 2026
Mercer's brand 6 ICE CREAM SANDWICHES TO GO; packaged in clear plastic; ice cream sandwiches may be rolled in peanuts which are visible through product packaging Ingredients: Cream, sugar, nonfat milk, whey, cocoa (alkalized), stabilizer (guar gum, carrageenan), chocolate wafer (wheat flour, sugar,
Quality Dairy Farms Inc.
Undeclared peanuts FDA Class II recall.
- FDAAug 23, 2026
Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506
International Sprout Holdings, Inc
Potential E. coli and Salmonella contamination FDA Class I recall.
- FDAAug 22, 2026
Everything Sprouts and Calco branded Alfalfa Sprouts, Net Wt. 5.0 oz (142 g) UPC 7 68944-00005 9. The 5 oz. containers are distributed as single units, or in a tray with 6 - 5oz containers that contains UPC 8 60014-52312 0 label on bottom of tray, or in a try with 12 - 5 oz. containers that contains
Everything Sprouts, LLC
Sprouts may be contaminated with STEC E. coli and/or Salmonella. FDA Class I recall.
- FDAAug 22, 2026
Everything Sprouts Crunchy Protein Sprout Mix, containing Alfalfa Fenugreek, Cabbage, Mung, Adzuki, Lentils, Green Pea, Net Wt. 5.0 oz (142 g) UPC 0 87906-01018 7. everythingsprouts.com
Everything Sprouts, LLC
Sprouts may be contaminated with STEC E. coli and/or Salmonella. FDA Class I recall.
- FDAAug 22, 2026
Everything Sprouts Zesty Garlic Mix, containing Garlic, Onion and Alfalfa Sprouts, Net Wt. 5.0 oz (142 g) UPC 0 87906-00016 7. everythingsprouts.com
Everything Sprouts, LLC
Sprouts may be contaminated with STEC E. coli and/or Salmonella. FDA Class I recall.
- FDAAug 22, 2026
Everything Sprouts Robust Radish Mix, Net Wt. 5.0 oz (142 g) UPC 0 87906-00007 5. Keep Refrigerated. everythingsprouts.com
Everything Sprouts, LLC
Sprouts may be contaminated with STEC E. coli and/or Salmonella. FDA Class I recall.
- FDAAug 20, 2026
Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7, HEMO-10, HEMO-7-EU, HEMO-10-EU Software Version: N/A Product Description: Hemostatic device for endoscopic gastrointestinal use Component: No
Wilson-Cook Medical Inc.
Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU). FDA Class II recall.
- FDAAug 20, 2026
CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes: 21-7600-24, 21-7609-24 OUS Product Codes: 21-7609-24 21-7600-24 21-7600-24 21-7600-24 21-7609-24 21-7609-24 21-7600-24 21-7600-24 21-7609-24 21-7609-24 21-7600-24 21-7600-24 21-7609-24 21-7600-24 21-7600-24 21-7609-24 2
ICU Medical, Inc.
Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, exposure to infectious or toxic agents, or air embolus. FDA Class II recall.
- FDAAug 19, 2026
Martina brand Fresh Whole Mangoes; Individual whole mangoes, variable weight; 9 mangoes per carton box
Panorama Produce Sales Inc.
Product may be contaminated with Salmonella FDA Class II recall.
- FDAAug 19, 2026
REF:B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X100MM
Stryker Sustainability Solutions
Reusable access port system may crack or seperate during use. FDA Class II recall.
- FDAAug 19, 2026
REF:B12LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 12X100MM
Stryker Sustainability Solutions
Reusable access port system may crack or seperate during use. FDA Class II recall.
- FDAAug 19, 2026
REF:B11LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 11X100MM
Stryker Sustainability Solutions
Reusable access port system may crack or seperate during use. FDA Class II recall.
- FDAAug 19, 2026
REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM
Stryker Sustainability Solutions
Reusable access port system may crack or seperate during use. FDA Class II recall.
- FDAAug 19, 2026
REF:B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X75MM
Stryker Sustainability Solutions
Reusable access port system may crack or seperate during use. FDA Class II recall.
- FDAAug 19, 2026
NOxBOXi Nitric Oxide Delivery System.
NOXBOX LTD
Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation. FDA Class II recall.
- FDAAug 19, 2026
BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 SmartSite Y-sites 10015861A 10885403232626 50885403232624 BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing, Back Check Valve, 3 SmartSi
BD SWITZERLAND SARL
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance. FDA Class I recall.
- FDAAug 19, 2026
REF:2B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 100MM
Stryker Sustainability Solutions
Reusable access port system may crack or seperate during use. FDA Class II recall.
- FDAAug 18, 2026
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
Olympus Corporation of the Americas
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. FDA Class II recall.
- FDAAug 18, 2026
Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces FDA Class II recall.
- FDAAug 18, 2026
Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces FDA Class II recall.
- FDAAug 18, 2026
Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 041548612041, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces FDA Class II recall.
- FDAAug 18, 2026
Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces FDA Class II recall.
- FDAAug 18, 2026
Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces FDA Class II recall.
- FDAAug 18, 2026
Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 041548816678, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces FDA Class II recall.
- FDAAug 17, 2026
PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS: WHOLE GRAIN OATS, MILK, MARGARINE***WATER, SALT, CONTAINS LESS THAN 2% OF THE FOLLOWING: SOY LECITHIN, VEGETABLE MONO & DIGLYCERIDES, POTASSIUM SORBATE***, CITRIC ACID, NATURAL & ARTIFICIAL FLAVOR, BETA CAROTENE, VITAMIN A PALMITATE ADDED, PEA
Best Friends Bakery, LLC
Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product. FDA Class II recall.
- FDAAug 14, 2026
Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz
Ferrero USA
Undeclared milk and pecans FDA Class II recall.
- FDAAug 14, 2026
Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7
Gifford's Dairy, Inc.
Potential foreign object contamination: rubber pieces FDA Class II recall.
- FDAAug 14, 2026
THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS + MORINGA; SUPPORTS + PROMOTES HEALTHY LACTATION; INGREDIENTS Organic Gluten Free Oats Organic Maple Syrup Organic Pumpkin Seeds Organic Coconut Oil Almond Butter Almonds Organic Cocon
THE HAMPTON GROCER
Product may be contaminated with Salmonella. FDA Class I recall.
- FDAAug 13, 2026
Prince ITALIAN BREAD; Sesame; ITALIAN & FRENCH BREAD, LARGE; NET WEIGHT 12 OZ. (340g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FLOUR< NIACIN, FERROUS SULFATE, THIAMINE MONONITRATE, RIBOFLAVIN, FOLIC ACID, POTASSIUM BROMATE), WATER, YEAST, SALT, VEGETABLE SHORTENING (PARTIALLY
Prince Bakery Inc
Sesame is not declared in the ingredient statement but is declared in the statement of identity. FDA Class III recall.
- FDAAug 13, 2026
Prince PAN DE MANTECA; SPANISH STYLE; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FLOUR, NIACIN, FERROUS SULFATE, THIAMIN MONONITRATE, RIBOFLAVIN, FOLIC ACID, POTASSIUM BROMATE), WATER, YEAST, SALT, VEGETABLE SHORTENING (PARTIALLY HYDROGENATED SOYBEAN, COT
Prince Bakery Inc
Milk is not declared in the Contains statement. FDA Class II recall.
- FDAAug 13, 2026
Prince ITALIAN BREAD; Sesame; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FLOUR, NIACIN, FERROUS SULFATE, THIAMIN MONONITRATE, RIBOFLAVIN, FOLIC ACID, POTASSIUM BROMATE), WATER, YEAST, SALT, VEGETABLE SHORTENING (PARTIALLY HYDROGENATED SOYBEAN, COTTONSEED,
Prince Bakery Inc
Sesame is not declared in the ingredient statement but is declared in the statement of identity. FDA Class III recall.
- FDAAug 13, 2026
Prince Sesame FRENCH BREAD; LONG FRENCH; Net Wt. 10 oz (284g); INGREDIENTS: ENRICHED BLEACHED FLOUR, (WHEAT FLOUR, MALT BARLEY FLOUR< NIACIN, FERROUS SULFATE, THIAMIN MONONITRATE, RIBOFLAVIN, FOLIC ACID, POTASSIUM BROMATE), WATER, YEAST, SALT, VEGETABLE SHORTENING (PARTIALLY HYDROGENATED SOYBEAN, CO
Prince Bakery Inc
Sesame is not declared in the ingredient statement but is declared in the statement of identity. FDA Class III recall.
- FDAAug 12, 2026
Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, IN; Product Code: 0042-0000-IN. 4
Abiomed, Inc.
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. FDA Class I recall.
- FDAAug 12, 2026
Impella Optical Controller with the below product descriptions and corresponding Product Codes. 1. Impella Optical Controller, Packaged, AU; Product Code: 0042-0010-AU. 2. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU. 3. Impella Optical Controller, Packaged, IN; Product Code:
Abiomed, Inc.
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. FDA Class I recall.
- FDAAug 12, 2026
Impella Optical Controller, Automated Impella Controller, Impella Connect Package with the below product descriptions and corresponding Product Codes. 1. Optical, AIC, Impella Connect, Packaged, AU; Product Code: 0042-0040-AU. 2. Optical, AIC, Impella Connect, Packaged, CA; Product Code: 0042-0040-C
Abiomed, Inc.
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. FDA Class I recall.
- FDAAug 12, 2026
GM Helix Implant, REF: 109.984;
Straumann USA LLC
There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside. FDA Class II recall.
- FDAAug 12, 2026
Product is Potato Sourdough Bread and sold under three following names: Potato Market Loaf 20oz. UPC 733163001576, product is sold at grocery stores with paper packaging. Label declares Potato Grand Central Rustic Breads ***A hearty sourdough loaf made with house-roasted potatoes. ***" Potato Table
Grand Central Bakery - Oregon Inc. dba Grand Central Bakery, Inc.
Foreign object: May contain metal pieces FDA Class II recall.
- FDAAug 11, 2026
Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: DYKM2187A
Medline Industries, LP
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.
- FDAAug 11, 2026
Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
Medline Industries, LP
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.
- FDAAug 11, 2026
Medline Convenience Kits: 1) DYNDH1193, Catalog Number: DYNDH1193; 2) DYNDH1487A, Catalog Number: DYNDH1487A
Medline Industries, LP
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.
- FDAAug 11, 2026
Medline Convenience Kits: 1) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM CDS, Catalog Number: CDS983672O; 3) NON STERILE CHEST TUBE REMOVAL, Catalog Number: DYNDA1080
Medline Industries, LP
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.
- FDAAug 11, 2026
Medline Convenience Kits: 1) DYNDB3086D, Catalog Number: DYNDB3086D; 2) DYNDB3100, Catalog Number: DYNDB3100; 3) DYNDH1619A, Catalog Number: DYNDH1619A; 4) DYNDH1620A, Catalog Number: DYNDH1620A; 5) DYNDH1694A, Catalog Number: DYNDH1694A; 6) DYNDH1695, Catalog Number: DYNDH1695; 7) DYNDH1708A, Catal
Medline Industries, LP
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.
- FDAAug 11, 2026
Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Number: ACC010374A; 3) ACC010679, Catalog Number: ACC010679; 4) ACC010726A, Catalog Number: ACC010726A; 5) DYNDB3061, Catalog Number: DYNDB3061; 6) DYNDH1245, Catalog Number: DYNDH1245; 7) DYNDH1362, Catalog
Medline Industries, LP
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.
- FDAAug 11, 2026
Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414; 2) ARTERIAL LINE ST JOES SYR PACK, Catalog Number: DYNJ38145F
Medline Industries, LP
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.
- FDAAug 11, 2026
Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14 OZ (397g), with UPC 1 94346474004. Must Keep Refrigerated.
CUISINE, KETTLE
Product had a presumptive positive test result for Listeria monocytogenes FDA Class II recall.
- FDAAug 11, 2026
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Baxter Healthcare Corporation
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains. FDA Class II recall.
- FDAAug 11, 2026
Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
Byron White Formulas, Inc.
Label does not declare walnuts in English FDA Class II recall.
- FDAAug 11, 2026
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
Byron White Formulas, Inc.
Label does not declare walnuts in English FDA Class II recall.
- FDAAug 11, 2026
Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
Byron White Formulas, Inc.
Label does not declare walnuts in English FDA Class II recall.
- FDAAug 11, 2026
Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL
Baxter Healthcare Corporation
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains. FDA Class II recall.
- FDAAug 10, 2026
Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;
AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. FDA Class I recall.
- FDAAug 10, 2026
Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03;
AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. FDA Class I recall.
- FDAAug 10, 2026
Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;
AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. FDA Class I recall.
- FDAAug 10, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605240; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605300; Power-Trialysis Short-Te
Bard Access Systems, Inc.
this is a downstream recall of class I recall RES 98777 FDA Class I recall.
- FDAAug 10, 2026
Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;
AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. FDA Class I recall.
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