Medline recalls convenience kits with plastic syringes that may leak or break, posing health risks. Affected kits include NERVE BLOCK TRAY-LF and PERIPHERAL NERVE BLOCK models with specific pack 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 convenience kits containing plastic syringes that may leak or break, which could harm patients. These kits are used in medical settings for nerve blocks and have specific model and lot numbers listed in the recall.
The plastic syringes in these kits can leak or break due to quality issues identified by the FDA. This poses a risk to patient health as leaks or breaks could lead to contamination or injury during medical procedures.
Healthcare providers and medical facilities using Medline convenience kits for nerve blocks are most at risk. Patients using these kits for procedures may also be affected if the syringes leak or break.
Check for kits labeled 'NERVE BLOCK TRAY-LF' with pack number DYNJRA0377B or 'PERIPHERAL NERVE BLOCK' with specific pack numbers and lot numbers listed in the recall notice.
Look for the product name and pack number on the kit label to determine if it matches the recalled models.
The FDA identified leaks and breakage issues in the plastic syringes that could pose a risk to patient health during medical procedures.
Affected kits include NERVE BLOCK TRAY-LF (Pack Number DYNJRA0377B) and PERIPHERAL NERVE BLOCK with specific pack numbers and lot numbers listed in the recall notice.
The recall does not require immediate stop use; however, affected kits should be checked and replaced if they match the listed models.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2988-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2988-2024 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.
