Mozarc Medical recalls 12 Fr/Ch catheter tray extensions due to potential packaging seal issues. Affected units have specific lot numbers and UDI-DI codes. Consumers should check their product details to determine if recalled.
A potential issue with the seal integrity of header bag packaging.
Mozarc Medical is recalling certain acute high pressure catheter tray extensions because of a potential issue with the packaging seal. This could lead to problems with the product's integrity during use, though the risk is not described as causing serious injury.
The packaging seal might not hold properly, which could allow contaminants to enter the product. This could potentially affect the sterility of the catheter tray extensions during medical procedures.
Healthcare professionals using the catheter tray extensions for medical procedures are most likely affected. Patients receiving these treatments may also be impacted if the product is used without proper packaging integrity.
Check for the product name 'Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm'. Look for the lot number 2418000195 or UDI-DI codes 10884521127999 (individual unit) and 20884521127996 (carton).
Identify the product by checking the lot number 2418000195 or UDI-DI codes 10884521127999 (individual unit) and 20884521127996 (carton).
The recall states a potential issue with packaging seal integrity, but does not indicate that the product is dangerous if used correctly.
Check for the lot number 2418000195 or UDI-DI codes 10884521127999 (individual unit) and 20884521127996 (carton) on the product.
The recall does not specify a remedy, so no action is required beyond checking if your product matches the described details.
We’ve drafted a message you can send Mozarc Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0424-2026 — Mozarc Medical Mozarc Medical Hello, I own a Mozarc Medical that is covered by recall Z-0424-2026 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.
