Mozarc Medical recalls Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components due to potential packaging seal issues. Affected units have specific lot numbers and reference codes.
A potential issue with the seal integrity of header bag packaging.
Mozarc Medical is recalling certain Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components because of a potential issue with the seal integrity of the header bag packaging. This could lead to compromised packaging that might affect the product's safety.
The packaging seal may not hold properly, potentially allowing contaminants to enter the product. This could lead to infection risks for patients during medical procedures if the packaging is compromised.
Healthcare professionals using these catheter tray extensions in medical settings are most likely affected. Patients receiving care with these products may be at risk if the packaging seal is compromised.
Check for the reference number 8888102004HP or lot number 242450: 2424500197 on the packaging. The product is sold as a 12 Fr/Ch (4.0 mm) x 24 cm catheter tray extension with IC components.
Look for the reference number 8888102004HP or lot number 2424500197 on the packaging to confirm if the product is affected.
The recall states there is a potential issue with the seal integrity of the header bag packaging, which could allow contaminants to enter the product. However, the specific risk level is not detailed in the recall notice.
Check for the reference number 8888102004HP or lot number 2424500197 on the packaging. The product is a 12 Fr/Ch (4.0 mm) x 24 cm catheter tray extension with IC components.
The recall does not specify a remedy, so there is no action required beyond checking the packaging details to confirm if the product is affected.
We’ve drafted a message you can send Mozarc Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0425-2026 — Mozarc Medical Mozarc Medical Hello, I own a Mozarc Medical that is covered by recall Z-0425-2026 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.
