Medline recalls convenience kits with potentially contaminated components. Affected kits include CMH LITHO MINOR PACK-LF, EAST MAJOR LITHOTOMY, GYN LAPAROTOMY, and UNIVERSAL GYN models. Consumers should check their kit's SKU and lot number for recall.
Kits contain a potentially contaminated component which were recalled by the manufacturer
Medline is recalling several convenience kits that contain a potentially contaminated component. This recall is important because using these kits could pose a risk of contamination, which might lead to health issues.
The kits contain a component that may be contaminated, which could lead to health risks if the component is used in medical procedures. Contamination in medical kits can cause infections or other health complications.
Healthcare professionals and medical facilities that use Medline convenience kits are most at risk. Individuals with the specific kit models and lot numbers listed in the recall are affected.
Check the kit's SKU number and lot number. Affected kits include CMH LITHO MINOR PACK-LF (SKU DYNJ54362F, Lot 26EMF986), EAST MAJOR LITHOTOMY (SKU DYNJ900957C, Lot 25IBP434), GYN LAPAROTOMY (SKU DYNJ906804B, Lot 26BBA665), and UNIVERSAL GYN (SKU DYNJ910195A, Lot 25KBL876).
Identify your kit's SKU and lot number to see if it matches the recalled models.
The recall is due to a potentially contaminated component in the kits, which could lead to health risks if used in medical procedures.
Affected kits include CMH LITHO MINOR PACK-LF (SKU DYNJ54362F, Lot 26EMF986), EAST MAJOR LITHOTOMY (SKU DYNJ900957C, Lot 25IBP434), GYN LAPAROTOMY (SKU DYNJ906804B, Lot 26BBA665), and UNIVERSAL GYN (SKU DYNJ910195A, Lot 25KBL876).
Check your kit's SKU and lot number to confirm if it's affected. If it is, 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-3028-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-3028-2026 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.
