Mozarc Medical recalls Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components (12 Fr/Ch) due to potential packaging seal issues. Affected units have specific lot numbers and reference codes. No immediate action is required as the hazard is not in active use.
A potential issue with the seal integrity of header bag packaging.
Mozarc Medical is recalling Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components (12 Fr/Ch) because of a potential issue with the seal integrity of the header bag packaging. This recall does not pose an immediate risk to users since the packaging issue is not active during normal use.
The header bag packaging may have seal integrity issues, which could potentially lead to contamination or leakage of the catheter components. However, the hazard is not active during normal medical use and does not pose a risk to patients or users.
Healthcare professionals who use these catheter tray extensions in medical settings may be affected. The risk is low as the packaging issue does not impact active use.
Check for the reference number 8888101003HP and lot numbers 2424500194 or 2430500018 on the packaging. The product is sold as a medical device for use in healthcare settings.
Look for the reference number 8888101003HP and lot numbers 2424500194 or 2430500018 on the packaging to confirm if the product is affected.
No, the recall is for packaging seal integrity issues that do not affect active use, so there is no immediate risk to patients.
No, the recall does not require stopping use as the hazard is not active during normal medical procedures.
Check the packaging for the reference number 8888101003HP and lot numbers 2424500194 or 2430500018.
We’ve drafted a message you can send Mozarc Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0423-2026 — Mozarc Medical Mozarc Medical Hello, I own a Mozarc Medical that is covered by recall Z-0423-2026 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.
