Medline recalls 84 procedure kits labeled with specific pack numbers and lot numbers due to plastic syringes that may leak or break, posing a risk to patient health. No remedy specified in official notice.
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 84 different procedure kits that contain plastic syringes affected by a FDA safety alert. These kits may leak or break, which could harm patients. The recall is based on identified quality issues from the FDA alert.
The plastic syringes in these kits have been identified by the FDA as having leaks or breakage issues. This could lead to contamination or injury to patients during medical procedures.
Healthcare professionals and medical facilities that use these procedure kits are likely affected. Patients using these kits during procedures may be at risk if the syringes leak or break.
Check for the specific pack numbers listed in the recall (e.g., DYNJHS0136D, DYNJ56987B) and lot numbers (e.g., 22JBC557Z) on the kit labels. The kits are labeled with product names like A & A KNEE PACK-LF or ABD CLOSURE PACK.
Look for the specific pack numbers and lot numbers listed in the recall on the kit labels to determine if your kit is affected.
The FDA issued a safety alert about plastic syringes in these kits that may leak or break, posing a risk to patient health.
Check the kit label for the specific pack numbers and lot numbers listed in the recall (e.g., DYNJHS0136D with lot number 22JBC557Z).
The official 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-1444-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1444-2025 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.
