Medline recalls convenience kits labeled BIOPSY TRAY-LF with pack number DYNDH1229 due to potential leaks and breakage that could harm patient health.
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 labeled BIOPSY TRAY-LF with pack number DYNDH1229 because plastic syringes in these kits may leak or break, posing a risk to patient health. This could lead to potential health hazards if the kits are used improperly.
The plastic syringes in these kits may leak or break, which could lead to potential health hazards for patients. This risk is related to the FDA Safety Alert issued in March 2024, indicating quality issues with the syringes.
Healthcare professionals using these kits in medical settings are most at risk. Patients receiving care with these kits could also be affected if the kits malfunction.
Check for kits labeled 'BIOPSY TRAY-LF' with pack number DYNDH1229 or lot number 22FBA002. These kits were sold by Medline Industries, LP in Northfield.
Look for the label 'BIOPSY TRAY-LF' and pack number DYNDH1229 or lot number 22FBA002 on the kit.
The FDA Safety Alert issued on March 19, 2024 identified leaks and breakage risks in the plastic syringes used in these kits.
The recall record does not specify a remedy, so check with Medline Industries for further instructions.
Yes, the plastic syringes may leak or break, which could pose a risk to patient health.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3058-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3058-2024 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.
