Medline recalls convenience kits with plastic syringes that may leak or break, posing health risks. Affected kits include specific models and pack numbers. Consumers should check their kits and contact Medline for details.
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 that contain plastic syringes which may leak or break, potentially harming patients. This recall affects kits with specific model numbers and pack identifiers listed in the notice.
The plastic syringes in these kits can leak or break due to quality issues identified by the FDA. This may lead to health risks for patients if the kits are used improperly or if the syringes are damaged.
Healthcare workers and patients using these kits are most at risk. The recall targets specific Medline convenience kits sold with certain model numbers and pack identifiers.
Check for kits labeled with model numbers like SH STRL UMBILICAL ACC PACK-LF, Pack Number DYNJ0621408V, or similar identifiers listed in the recall notice. The affected kits also include specific lot numbers such as 23ILB053.
Look for model numbers and pack numbers listed in the recall notice to determine if your kit is affected.
The recall states that these kits may leak or break, posing a risk to patient health. Affected kits should not be used until the remedy is applied.
The recall does not specify a remedy, so contact Medline directly for instructions on how to handle affected kits.
Check the kit label for model numbers like SH STRL UMBILICAL ACC PACK-LF or pack numbers such as DYNJ0621408V.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3036-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3036-2024 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.
