Medline recalls 22 procedure kits with plastic syringes that may leak or break, posing health risks. Affected kits include CLOVIS ROBOTIC-LF and others with specific pack numbers. Consumers should check their kits for the listed identifiers.
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 22 different procedure kits that contain plastic syringes which may leak or break, potentially causing health risks to patients. These kits are used in medical settings and are labeled with specific pack numbers and lot codes.
The plastic syringes in these kits can leak or break, which may lead to patient health issues. This problem was identified through an FDA safety alert from March 19, 2024.
Medical professionals and facilities using the recalled procedure kits are most at risk. Patients using these kits during procedures may be affected if the syringes leak or break.
Check for the specific pack numbers listed in the recall notice, such as DYNJ61061D for CLOVIS ROBOTIC-LF kits. Also look for the lot numbers like 23GMD257A on the packaging.
Look for the pack numbers and lot numbers listed in the recall notice to determine if your kit is affected.
The recall includes 22 specific procedure kits with pack numbers like DYNJ61061D (CLOVIS ROBOTIC-LF) and others listed in the notice.
The plastic syringes in these kits may leak or break, which could pose a risk to patient health as identified by the FDA safety alert.
The recall does not specify a stop-use instruction, so you can continue using them but should check 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-1447-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1447-2025 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.
