Medline recalls specific PREOP NERVE BLOCK TRAY kits with pack number DYNJRA2040H due to potential leaks or breakage that could harm patients. Affected kits include certain lot numbers from March 2024.
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 procedural kits labeled PREOP NERVE BLOCK TRAY with pack number DYNJRA2040H. These kits have plastic syringes that may leak or break, posing 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 linked to FDA safety alerts about quality issues in medical devices.
Healthcare professionals using these kits for nerve block procedures are most at risk. Patients receiving these procedures may be affected if the kits are used improperly.
Check for the pack number DYNJRA2040H on the kit label. Affected kits include specific lot numbers: 23CBH893, 23HBX547, 23JBN538, 24ABQ696, and 24CBG746.
Look for the pack number DYNJRA2040H and the listed lot numbers to confirm if your kit is affected.
The plastic syringes in these kits may leak or break, which could pose a risk to patient health during medical procedures.
Check for the pack number DYNJRA2040H and lot numbers 23CBH893, 23HBX547, 23JBN538, 24ABQ696, or 24CBG746 on the label.
The recall does not require immediate stop use; affected kits should be checked for the specific lot numbers listed.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2741-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2741-2024 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.
