MEDLINE recalls surgical convenience kits where the outer wrap isn't sterile, risking infection. Affected kits have specific labels and reorder numbers.
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
MEDLINE is recalling surgical convenience kits because the outer bag isn't sterile. This means only the contents inside the bag are sterile, increasing infection risk during procedures.
The perforated bag means the outer wrapping isn't sterile. Only the contents inside the bag are sterile, so the entire kit isn't safe for surgical use. This could lead to infections if the kit isn't properly sterilized.
Healthcare professionals using these kits for surgeries or procedures. Patients undergoing surgery with these kits face higher infection risks.
Check for the label: MEDLINE ARM/MINOR DRAPE CSTM. Look for Reorder Number DYNJCD0063 or GTIN 40884389462011. Lot # 22GBF090 may also be present.
Look for the label MEDLINE ARM/MINOR DRAPE CSTM and reorder number DYNJCD0063.
The recall is due to the perforated bag not allowing the outside of the kit wrapping to be sterile, so only the contents inside the bag are sterile.
Check for the label MEDLINE ARM/MINOR DRAPE CSTM, reorder number DYNJCD0063, GTIN 40884389462011, or lot number 22GBF090.
The recall record doesn't specify a remedy, so contact MEDLINE for guidance.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-1125-2023 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-1125-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
