Medline recalls specific convenience kits due to potential leaks and breakage in plastic syringes, which could harm patients. Affected kits include models with pack numbers DYND30212, DYNJ65728A, and others.
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 certain convenience 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 may leak or break, potentially causing contamination or injury to patients during medical procedures. This risk is linked to FDA safety alerts about quality issues with the syringes.
Healthcare workers and patients using these kits for medical procedures are most at risk. The recall affects specific models sold in the U.S. market.
Check for kit labels with pack numbers like DYND30212, DYNJ65728A, or DYNJ82155A. The kits were sold with specific lot numbers such as 20CBV412 or 23JBP679.
Look for pack numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
Reach out to Medline for assistance with returning or replacing the affected kits.
The recall is due to potential leaks and breakage in plastic syringes, which could harm patients during medical procedures.
Kits with pack numbers DYND30212, DYNJ65728A, DYNJ82155A, DYNJ58575C, and others, as listed in the recall notice.
No, but you should check if your kit is affected and contact Medline for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3034-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3034-2024 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.
