Mozarc Medical recalls specific catheter tray extensions due to potential packaging seal issues. Affected units may have compromised packaging that could lead to contamination risks during medical procedures.
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 contamination risks during medical procedures if the packaging is compromised.
The packaging seal may not hold properly, potentially allowing contaminants to enter the device during medical procedures. This could lead to contamination risks if the packaging is compromised.
Healthcare professionals using the specific catheter tray extensions for medical procedures are most at risk. Patients receiving procedures with these devices may be affected if the packaging is compromised.
Check for the REF Number 8888101002HP or UDI-DI numbers 10884521127968 (individual) and 20884521127965 (carton). The lot number 2430500017 is also associated with this recall.
Inspect the packaging for any signs of damage or compromised seals before use.
The recall is for medical devices used by healthcare professionals. Patients are not directly affected unless the device is used in a procedure with compromised packaging.
Look for the REF Number 8888101002HP or UDI-DI numbers 10884521127968 (individual) and 20884521127965 (carton). The lot number 2430500017 is also associated with this recall.
Inspect the packaging for any signs of damage or compromised seals before use. No specific action is required beyond this check as the remedy is not stated in the recall.
We’ve drafted a message you can send Mozarc Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0422-2026 — Mozarc Medical Mozarc Medical Hello, I own a Mozarc Medical that is covered by recall Z-0422-2026 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.
