Medline recalls shoulder suspension surgical kits due to perforated bags that compromise sterile wrapping. Only inner kit contents remain sterile, risking infection during procedures.
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 shoulder suspension surgical kits because the packaging has a perforation that prevents the outside from staying sterile. This means only the contents inside the kit's wrapping are sterile, increasing infection risk during surgery.
The kits' bags have a perforation that allows non-sterile materials to contact the outside of the packaging. This means only the contents inside the wrapping remain sterile, while the outer layers may become contaminated during handling.
Surgical teams using Medline shoulder suspension kits with reorder number DYNJSHOULDER are affected. Patients undergoing surgery with these kits face potential infection risks due to compromised sterility.
Check for kits labeled 'MEDLINE SHOULDER SUSPENSION I-LF' with reorder number DYNJSHOULDER. The kit also has GTIN 10080196597383 and lot number 22DBN321.
Look for the label 'MEDLINE SHOULDER SUSPENSION I-LF' with reorder number DYNJSHOULDER.
The recall is due to perforated bags that prevent the outside of the packaging from staying sterile, meaning only the contents inside the wrapping remain sterile.
Check for kits labeled 'MEDLINE SHOULDER SUSPENSION I-LF' with reorder number DYNJSHOULDER, GTIN 10080196597383, or lot number 22DBN321.
The recall record does not specify a remedy, so contact Medline directly 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-1122-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1122-2023 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.
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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.
