Fresenius Medical Care recalls Stay-Safe Luer Lock Catheter Ext 18 in due to potential leachables in tubing. Affected units have specific model and lot numbers. Consumers should contact the company for details.
The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Fresenius Medical Care is recalling Stay-Safe Luer Lock Catheter Ext 18 in products because the tubing may contain leachables identified as NDL PCBAs. This could pose a health risk if the tubing comes into contact with bodily fluids.
The tubing in the catheter may leach NDL PCBAs, which are chemicals that could potentially interact with bodily fluids. This could lead to health risks if the tubing is in contact with the body during medical procedures.
Healthcare professionals and patients using the Stay-Safe Luer Lock Catheter Ext 18 in for medical procedures are likely affected. Those with the specific model and lot numbers are at risk.
Check for the model number 050-95005 and lot numbers 00840861100798 (bag) or 10840861100795 (case) on the product packaging.
Reach out to Fresenius Medical Care Holdings, Inc. for specific instructions on how to handle the recalled product.
The model number is 050-95005.
Lot numbers 00840861100798 (bag) and 10840861100795 (case) are affected.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Fresen: Medical Care to request your refund or repair — edit it as you like.
Subject: Recall Z-1326-2024 — Fresen: Medical Care Fresen: Medical Care Hello, I own a Fresen: Medical Care that is covered by recall Z-1326-2024 from Fresen: Medical Care. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
