Medline recalls Centurion procedure packs with affected Caina syringes due to leaks and breakage risks. Patients may face health issues from these faulty medical kits.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline is recalling Centurion procedure packs that include Caina syringes with potential leaks and breakage. This poses a risk to patient health during medical procedures.
The syringes in these procedure packs have been identified by the FDA as having leaks and breakage issues. These problems could lead to patient health risks during medical procedures.
Healthcare providers using these procedure packs for medical procedures are most at risk. Patients receiving care with these kits could be affected if the syringes leak or break.
Check for Centurion procedure packs labeled with specific pack names like ARTHROGRAPH TRAY (MNS12670A) or BREAST BIOPSY KIT (DYNDH1512A). Look for the lot numbers listed in the recall notice.
Look for the pack names and lot numbers listed in the recall notice to identify affected items.
Medline is recalling Centurion procedure packs that contain Caina syringes with potential leaks and breakage issues, which could pose a risk to patient health.
Check for Centurion procedure packs labeled with specific pack names like ARTHROGRAPH TRAY (MNS12670A) or BREAST BIOPSY KIT (DYNDH1512A) and the listed lot numbers.
The recall notice does not specify a remedy, so contact Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2775-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2775-2024 from Medline. 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.
