Medline recalls Centurion procedure packs with Caina syringes that may leak or break, posing health risks. Affected packs include specific labels and lot numbers.
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 that have been identified as leaking or breaking, which could harm patients. This recall affects specific product labels and lot numbers listed in the notice.
The syringes in these packs have been identified by the FDA as leaking or breaking, which could lead to patient health risks. This issue is related to the quality of the syringes and their potential to cause harm during medical procedures.
Medical professionals and patients using the recalled Centurion procedure packs with Caina syringes. Those most at risk are individuals handling the packs for procedures like circumcision or biopsies.
Check for labels like 'ARTHROGRAM' or 'CIRCUMCISION KIT' with specific pack numbers and lot numbers listed in the recall notice. The affected packs include detailed product names and their corresponding lot numbers.
Look for the product labels and lot numbers listed in the recall notice to confirm if your pack is affected.
The recall affects Centurion procedure packs with Caina syringes labeled as ARTHROGRAM, CIRCUMCISION KIT, and other specific products with the pack numbers and lot numbers listed in the notice.
Check the product label for the specific pack numbers and lot numbers listed in the recall notice, such as DYNDH1446A with lot number 2020102990.
The recall notice does not specify a remedy, so you should check the product labels to confirm if they are affected and contact Medline for further instructions.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2776-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2776-2024 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.
