Medline recalls convenience kits with plastic syringes that may leak or break, posing health risks. Check pack numbers and lot numbers for affected items.
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 used in medical procedures because their plastic syringes can leak or break, potentially harming patients. This affects specific kits with certain pack numbers and lot numbers.
The plastic syringes in these kits can leak or break, which may lead to contamination or injury to patients during medical procedures. This issue was identified through a recent FDA safety alert.
Healthcare professionals and medical facilities that use these kits for procedures like ureteroscopy or prostatectomy. Patients using these kits during medical procedures are at risk.
Check for kits labeled with specific product names like URETEROSCOPY CDS SC-LF or URETEROSCOPY TRAY-RF. Look for pack numbers and lot numbers listed in the recall notice.
Identify the product name and pack number on the kit to see if it matches the recalled items listed in the notice.
Reach out to Medline directly to confirm if your kit is affected and get instructions for next steps.
The plastic syringes in these kits can leak or break, posing a risk to patient health as identified by the FDA Safety Alert.
Check the product name and pack number on the kit. Affected kits include specific models like URETEROSCOPY CDS SC-LF with pack numbers starting with CDS983922F or DYNJ27442U.
The recall does not require immediate stop use; healthcare facilities should check if their kits are affected and contact Medline for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3005-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3005-2024 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.
