Medline recalls two convenience kits (FEMORAL PACK SKU DYNJ909393A and FEVAR SKU DYNJ910295D) due to potentially contaminated components. Affected kits have specific lot numbers and were sold in 2023-2024.
Kits contain a potentially contaminated component which were recalled by the manufacturer
Medline is recalling two specific convenience kits because they contain a potentially contaminated component. This could pose a health risk if the kits are used without proper cleaning or sterilization.
The kits contain a component that may be contaminated, which could lead to health risks if not properly cleaned or sterilized before use. The manufacturer identified this issue and recalled the kits to prevent potential harm.
Healthcare professionals and facilities using Medline convenience kits labeled as FEMORAL PACK (SKU DYNJ909393A) or FEVAR (SKU DYNJ910295D) are likely affected. Those using these kits without proper sterilization procedures are at higher risk.
Check for the kit labels: FEMORAL PACK with SKU DYNJ909393A or FEVAR with SKU DYNJ910295D. Lot numbers 25ILA297 for the first kit and 26CBT178 for the second kit indicate the affected batches.
Look for the specific SKU numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The manufacturer identified that the kits contain a potentially contaminated component which could pose a health risk if not properly cleaned or sterilized.
The recall notice does not specify a remedy, so you should check the kit labels to confirm if it is affected and contact Medline for further instructions.
Yes, affected kits have lot numbers 25ILA297 for SKU DYNJ909393A and 26CBT178 for SKU DYNJ910295D.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3019-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-3019-2026 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.
