Medline recalls blood culture and blood draw kits with specific pack numbers and lot numbers due to potential leaks and breakage that may harm patients. Affected kits include blood culture collection kits and NICU control line blood draw kits.
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 several blood collection and blood draw kits that may leak or break, posing a risk to patient health. These kits were sold with specific pack numbers and lot numbers identified in the recall notice.
The kits contain plastic syringes that can leak or break, potentially causing harm to patients during medical procedures. This issue was identified through FDA safety alerts and quality checks.
Healthcare professionals and patients who use these kits for blood collection or blood draws are likely affected. Those handling the kits in medical settings are at the highest risk.
Check for the product names: Blood Culture Collection Kit (Pack Number BP115) or NICU Control Line Blood Draw Kit (Pack Number DYLAB1044). Look for specific lot numbers listed in the recall notice.
Identify the pack number and lot number on the kit to see if it matches the recalled items listed in the notice.
The recall notice states that these kits may leak or break, posing a risk to patient health. They should not be used until the recall is addressed.
Check the pack number and lot number on the kit. Recalled kits include specific products like Blood Culture Collection Kit (Pack Number BP115) with lot numbers such as 21BBG338.
The recall notice does not specify a remedy, so you should check the kit details and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3059-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3059-2024 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.
