Mozarc Medical recalls hemodialysis catheter sport packs with potential sterile packaging breaches. Affected units have specific model and serial numbers. Consumers should contact the company for details.
Potential breach of sterile barrier packaging.
Mozarc Medical is recalling hemodialysis cath: sport packs that may have broken sterile packaging. This could let infections enter the body during dialysis treatments.
The sterile packaging might be breached, allowing bacteria to enter the catheter during dialysis. This could lead to infections in the bloodstream.
People using hemodialysis catheters with this specific sport pack model are affected. Those with the model number 8888133502 are most at risk.
Check for model number 8888133502 on the sport pack. The product has a unique identifier UDI: A8845210569201 and lot number 241760200.
Look for model number 8888133502, UDI A8845210569201, and lot number 241760200 on the sport pack.
The recall states there's a potential breach of sterile packaging, which could lead to infections during dialysis. However, the remedy is not specified, so it's not urgent to stop using.
The recall record doesn't specify a remedy, so contact Mozarc Medical directly for instructions.
Check for model number 8888133502, UDI A8845210569201, and lot number 241760200 on the sport pack.
We’ve drafted a message you can send Mozarc Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1889-2025 — Mozarc Medical Mozarc Medical Hello, I own a Mozarc Medical that is covered by recall Z-1889-2025 from Mozarc Medical. 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.
