Medline recalls anesthesia procedural kits with specific pack numbers and lot numbers for potential plastic syringe leaks or breakage that could harm patients.
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 anesthesia procedural kits that contain plastic syringes with known issues. These kits may leak or break, posing a risk to patient health during medical procedures.
The plastic syringes in these kits have been identified as leaking or breaking, which could lead to patient health risks during medical procedures. This issue was highlighted in a recent FDA safety alert.
Healthcare providers using these kits for anesthesia procedures are most at risk. Patients receiving care with these kits could be affected if the syringes leak or break.
Check for kits labeled 'ANESTHESIA CIRCUIT PEDS-LF' with pack numbers DYNJAA0327F or DYNJAA0327G and specific lot numbers listed in the recall notice.
Look for the specific pack numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall is due to plastic syringes in the kits leaking or breaking, which could pose a risk to patient health as identified in a recent FDA safety alert.
The official recall notice does not specify a remedy or action steps beyond checking the labels for affected pack numbers and lot numbers.
Yes, the recall includes specific lot numbers such as 20LBV329, 21FBM358, 22CBY412, 22GBZ157, 22JBR268, 23BBL309, 23HBU238, 23KBB605, and 24CBJ211 for pack numbers DYNJAA0327G.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2739-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2739-2024 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.
