Medline recalls 15 types of procedure kits with plastic syringes that may leak or break, posing health risks. Affected kits have specific pack numbers 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 15 different procedure kits that contain plastic syringes which may leak or break, potentially causing health risks to patients. These kits were sold with specific pack numbers and lot numbers identified in the recall notice.
The plastic syringes in these kits can leak or break, which may lead to contamination or injury. This poses a risk to patient health during medical procedures, as the syringes are used for administering treatments or medications.
Healthcare professionals and patients using the recalled Medline procedure kits are at risk if the syringes leak or break during medical procedures. The risk is primarily for those handling the kits in clinical settings.
Check the pack number on the kit label, such as DYNJ50624A, DYNJ30501F, or DYNJ0954970G. Also look for the lot number, which starts with letters like 20BDB393A or 21HBP134A.
Look for specific pack numbers and lot numbers listed in the recall notice to determine if your kit is affected.
The recall is due to identified leaks and breakage in plastic syringes within the procedure kits, which may pose a risk to patient health.
Check the pack number and lot number on your kit to see if it matches the recalled items listed in the notice. If it does, you may need to stop using it.
Yes, the plastic syringes can leak or break, potentially causing contamination or injury during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1436-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1436-2025 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.
