Medline recalls 12 types of procedure kits with plastic syringes that may leak or break, posing patient health risks. Affected kits include specific pack numbers and lot numbers listed in the recall 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 12 different types of procedure kits that contain plastic syringes prone to leaks or breakage. This could pose a risk to patient health during medical procedures.
The plastic syringes in these kits can leak or break, potentially causing contamination or injury to patients during medical procedures. This risk is related to the quality issues identified by the FDA Safety Alert.
Healthcare professionals using Medline procedure kits for medical procedures are most at risk. Patients receiving care with these kits may be affected if the kits leak or break.
Check for kits labeled with specific pack numbers and lot numbers listed in the recall notice. The affected kits include items like CONTINUOUS BLOCK, COMBINED SPINAL AND EPIDURAL, and others with pack numbers starting with DYNJRA or PAIN.
Look for specific pack numbers and lot numbers listed in the recall notice to determine if your kit is affected.
The FDA Safety Alert identified leaks and breakage issues in the plastic syringes used in these kits, which could pose a risk to patient health.
Check the pack number and lot number on your kit against the list provided in the recall notice. Affected kits include specific types like CONTINUOUS BLOCK with pack numbers starting with DYNJRA0960C or PAIN1766A.
The recall notice does not specify a remedy, so you should check with Medline directly to determine next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2442-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2442-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
