Medline recalls procedure packs containing Shenli syringes with specific pack numbers and lot numbers due to leaks and breakage risks that could harm patients.
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 procedure packs that include Shenli syringes with certain pack numbers and lot numbers. These syringes may leak or break, posing 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 if the syringes are used during medical procedures.
Healthcare providers and patients using Medline procedure packs with Shenli syringes labeled with specific pack numbers and lot numbers listed in the recall. Those most at risk are individuals handling the syringes during medical procedures.
Check for procedure packs labeled with pack numbers DYNJ34129C, DYNJ54607A, or DYNJ61839B and specific lot numbers listed in the recall notice. The syringes are part of Medline's medical convenience kits.
Look for procedure packs labeled with pack numbers DYNJ34129C, DYNJ54607A, or DYNJ61839B and specific lot numbers listed in the recall.
The FDA has identified leaks and breakage issues in Shenli syringes that could pose a risk to patient health during medical procedures.
Check the pack numbers and lot numbers listed in the recall notice. If you have the affected items, you should stop using them and contact Medline for further instructions.
Yes, the recall includes specific lot numbers such as 21GBT130, 21LBL623, and others listed in the notice. Check the product labels for these numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2623-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2623-2024 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.
