Medline recalls 50+ medical convenience kits with plastic syringes that may leak or break, posing patient health risks. Affected kits include chest tube insertion trays and biopsy trays with 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 50+ medical convenience kits that contain plastic syringes prone to leaks or breakage. This could lead to patient health risks if the kits are used as intended.
The plastic syringes in these kits can leak or break, potentially causing patient health risks. This issue is linked to quality problems identified by the FDA Safety Alert from March 19, 2024.
Healthcare professionals and medical facilities that use these kits for procedures like biopsies or lumbar punctures are most at risk. Patients using these kits during medical procedures may be affected.
Check for kits labeled with specific pack numbers and lot numbers listed in the recall. Examples include CHEST TUBE INSERTION TRAY (Pack Number DYNDA2063) or BIOPSY TRAY (Pack Number DYNDH1137C).
Look for the specific pack numbers and lot numbers listed in the recall to identify affected kits.
The recall includes 50+ medical convenience kits such as chest tube insertion trays, biopsy trays, and lumbar puncture trays with specific pack numbers and lot numbers.
Check the pack number and lot number on your kit against the list provided in the recall. Affected kits include items like CHEST TUBE INSERTION TRAY (Pack Number DYNDA2063) or BIOPSY TRAY (Pack Number DYNDH1137C).
The recall does not specify a remedy, so you should check with Medline directly for guidance on handling affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3041-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3041-2024 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.
