Medline recalls 73 types of procedure kits containing plastic syringes that may leak or break, potentially harming patients. Kits labeled with specific pack numbers and lot numbers are affected.
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 73 different procedure kits that contain plastic syringes which may leak or break, posing a risk to patient health. These kits were sold with specific pack numbers and lot numbers identified in the recall.
The plastic syringes in these kits can leak or break, which may lead to patient health issues. This problem was identified through FDA safety alerts and quality checks.
Healthcare professionals and patients who use these procedure kits are likely affected. The risk is primarily for those handling the kits during medical procedures.
Check the pack number on the kit (e.g., DYNJ80088, DYNJ0131782J) and the lot number (e.g., 23DBG477A) to see if it matches the recalled items listed in the recall notice.
Look for the pack number and lot number on the kit to determine if it matches the recalled items listed in the recall notice.
The plastic syringes in these kits may leak or break, which could pose a risk to patient health. This issue was identified through FDA safety alerts and quality checks.
Check the pack number and lot number on the kit. If it matches the specific pack numbers and lot numbers listed in the recall notice, it is affected.
The recall notice does not specify a remedy, so you should check with Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1438-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1438-2025 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.
