Medline recalls 70+ convenience kits with plastic syringes that may leak or break, posing health risks. Stop using immediately to avoid potential injury.
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 70 different medical convenience kits that contain plastic syringes affected by a FDA safety alert. These kits may leak or break, which could harm patients. If you own any of these kits, stop using them immediately.
The plastic syringes in these kits have been identified by the FDA as having leaks, breakage, or quality issues. These problems could lead to patient injury during medical procedures.
Healthcare providers and medical facilities that use these kits are most at risk. Patients using the kits for procedures could be harmed by leaks or breaks.
Check for the product names listed in the recall (e.g., NERVE STIMULATOR, DR DIULUS INJECTION PACK) and the specific pack numbers or lot numbers provided in the list. The kits were sold with specific pack numbers and lot numbers.
Immediately stop using any Medline convenience kits with the listed pack numbers and lot numbers to avoid potential leaks or breaks that could harm patients.
Medline is recalling 70 different medical convenience kits that contain plastic syringes affected by a FDA safety alert. These kits may leak or break, posing health risks.
Check the product name and pack number on the kit. The recall includes specific kits like NERVE STIMULATOR (Pack Number CDS981579O) and DR DIULUS INJECTION PACK (Pack Number DYNDA2391), among others.
The recall does not specify a return process. The official notice says to stop using the kits immediately to avoid potential injury.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2635-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2635-2024 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.
