Medline recalls Centurion procedure packs with Caina syringes that may leak or break, posing health risks during medical procedures. Affected packs include NICU circumcision trays and retinal injection 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 containing Caina syringes due to leaks and breakage risks that could harm patients. These packs are used in medical settings like NICU circumcision and retinal injections.
The syringes in these packs may leak or break during use, potentially causing injury or infection. This risk is related to the quality issues identified in the FDA safety alert.
Healthcare providers using the Centurion procedure packs for medical procedures like circumcision and retinal injections are most at risk. Patients receiving care with these packs could be affected.
Check for packs labeled 'NICU CIRCUMCISION TRAY W/OUT CLAMP' (Pack Number CIT6920) or 'RETINAL INJECTION KIT' (Pack Number MNS12465). The lot numbers are 2021092290 and 2022040190 respectively.
Look for the pack number on the label: CIT6920 for circumcision trays or MNS12465 for retinal injection kits.
The recall states that leaks and breakage may pose a risk to patient health, so they are not safe to use until replaced.
The recall does not specify a remedy, so contact Medline directly for guidance on next steps.
Check the pack number: CIT6920 for circumcision trays or MNS12465 for retinal injection kits, with specific 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-2774-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2774-2024 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.
