Medline recalls 12 types of procedure kits with potential leaks and breakage that could harm patient health. Affected kits include delivery packs and labor delivery packs with specific pack numbers 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 12 types of medical procedure kits that contain plastic syringes prone to leaks and breakage. This could pose a risk to patient health if the kits are used improperly.
The plastic syringes in these kits can leak or break, which may lead to patient health risks. This issue was identified by the FDA in a safety alert from March 19, 2024.
Healthcare providers and medical facilities that use these procedure kits are most at risk. Patients using the kits during medical procedures may be affected if the kits leak or break.
Check for the following pack numbers: DYNJ0923016, DYNJ0968863M, DYNJ0373290N, DYNJ51998A, DYNJ0348455P, DYNJ23054J, DYNJ40096F, DYNJ83056, DYNJ27939D, DYNJ25843C, DYNJ43395, DYNJ0594115L. Also look for the corresponding lot numbers listed in the recall notice.
Review the pack number and lot number on the kit to confirm if it is affected by this recall.
The FDA identified leaks and breakage in the plastic syringes of these kits, which could pose a risk to patient health.
The recall does not specify a remedy, so check the pack number and lot number to see if it is affected. If it is, contact Medline for further instructions.
Yes, the affected kits include specific pack numbers and lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1446-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1446-2025 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.
