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FDA
Food and Drug Administration · Recall Z-2607-2026 · May 28, 2026

Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ901328G HEART A DYNJ903465K OPEN HEART DYNJ909090G SILVER CROSS OPEN HEART DYNJ906102M VPH OPEN HEART DYNJ902664M DYNJ902664N

Medline Industries, LP

The hazard

Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ901328G HEART A DYNJ903465K OPEN HEART DYNJ909090G SILVER CROSS OPEN HEART DYNJ906102M VPH OPEN HEART DYNJ902664M DYNJ902664N

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

UPC 10198459601538UPC 10198459292743UPC 10198459406027UPC 10198459406409UPC 10198459349126UPC 10198459675287

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.