Medline recalls convenience kits labeled for paracervical pudendal block with specific pack numbers due to potential leaks and breakage that could harm patients during medical procedures.
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 labeled for paracervical pudendal block procedures because they may leak or break, posing a risk to patient health. These kits are sold with specific pack numbers that have been identified as affected.
The kits contain plastic syringes that may leak or break, which could lead to patient health risks during medical procedures. This issue was identified through an FDA safety alert from March 19, 2024.
Healthcare providers using these kits for medical procedures are most at risk. Patients receiving treatments with these kits could be affected if the kits leak or break during use.
Check for kits labeled 'PARACERVICAL PUDENDAL BLOCK TR' with pack number DYNJRA1023 and specific lot numbers listed in the recall notice.
Look for the label 'PARACERVICAL PUDENDAL BLOCK TR' and pack number DYNJRA1023 with specific lot numbers listed in the recall.
The kits may leak or break, which could pose a risk to patient health during medical procedures.
Check for kits labeled 'PARACERVICAL PUDENDAL BLOCK TR' with pack number DYNJRA1023 and specific lot numbers listed in the recall notice.
The recall does not specify a stop-use instruction; you should check the labels to see if your kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3014-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3014-2024 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.
