Medline recalls Centurion procedure packs with affected Caina syringes due to leaks and breakage risks. Affected packs include Circumcision Tray (CIT6860A) and Retinal Injection Kit (MNS12465).
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 contain Caina syringes with potential leaks and breakage. This could pose a risk to patient health during medical procedures.
The syringes in these packs have been identified by the FDA as having leaks and breakage issues. These problems could lead to patient health risks during medical procedures.
Medical professionals using these procedure packs for circumcision or retinal injections are most at risk. Patients receiving procedures with these kits may also be affected.
Check for packs labeled 'CIRCUMCISION TRAY' with Pack Number CIT6860A or 'RETINAL INJECTION KIT' with Pack Number MNS12465. Lot numbers 2022011080 and 2021092780 are also associated with these items.
Look for the pack numbers and lot numbers listed in the recall notice to confirm if your item is affected.
The FDA has identified leaks and breakage issues with these syringes, so they are not safe for medical use.
The recall notice does not specify a remedy, so check with Medline Industries for further instructions.
Affected packs have specific labels: Circumcision Tray (CIT6860A) or Retinal Injection Kit (MNS12465) with the listed lot numbers.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2777-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2777-2024 from Medline Industries. 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.
