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Recall Observatory FDA recall evidence

Device product

stay-safe /Luer Lock Catheter Ext. 12 in

Z-1325-2024

January 23, 2024

Class I

Product summary

Firm
Fresenius Medical Care Holdings, Inc.
Event
Event 94084
Status
Ongoing
Classification
Class I
Quantity
663,221 eaches
Official record key
device-enforcement:Z-1325-2024

Official wording

Reason: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.

Code information: Model Number: 050-95004; UDI/DI (Bag): 00840861100781; UDI/DI (Case): 10840861100788; All lots.

Distribution pattern: Domestic: Nationwide Distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The peroxide cross-linked tubing has leachables identified as NDL PCBAs.