Mozarc Medical recalls Palindrome Precision SI Chronic Hemodialysis Catheter Sport Packs due to potential breach of sterile packaging. Affected units have specific model and serial numbers. Consumers should contact for details.
Potential breach of sterile barrier packaging.
Mozarc Medical is recalling certain Palindrome Precision SI Chronic Hemodialysis Catheter Sport Packs because the sterile packaging might be compromised. This could lead to infections if the catheter is used without proper sterility. Affected units have specific model and serial numbers listed in the recall.
The sterile packaging could be breached, potentially allowing contamination of the catheter. This might increase the risk of infection if the catheter is used without proper sterility. However, the recall does not specify a mechanism for serious injury.
Patients using hemodialysis treatments with the recalled catheter packs are most at risk. Healthcare providers who use these packs for medical procedures may also be affected.
Check for model numbers 8888133508P, 8888123408P, 8888119368P, or 8888128458P. Serial numbers listed include 2234800132, 2302500141, and others. The product is a radiopaque urethane catheter used in hemodialysis.
Verify the model and serial numbers against the list provided in the recall notice.
The recall states there is a potential breach of sterile packaging, which could lead to infection risk. However, the notice does not specify a mechanism for serious injury, so the risk is considered low.
Check the model numbers (8888133508P, 8888123408P, 8888119368P, 8888128458P) and serial numbers listed in the recall notice.
The recall does not specify a remedy, so contact Mozarc Medical directly for further instructions.
We’ve drafted a message you can send Mozarc Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1887-2025 — Mozarc Medical Mozarc Medical Hello, I own a Mozarc Medical that is covered by recall Z-1887-2025 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.
