Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mm
Biomet, Inc.
The hazard
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mm
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model UDI-DI (01)00887868507816(17)360221(10)67818764Model Lot 67818764 Model No 475630Model UDI-DI (01)00887868507816(17)360401(10)67818768Model Lot 67818768 Model No 475630Model UDI-DI (01)00887868507816(17)360428(10)67954534Model Lot 67954534UPC 00887868507816Would you have heard about this one?
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