ClearanceBrief
Recall Z-0280-2027 ยท PUI Drape, Surgical, Exempt

Medline Industries, LP

MEDLINE medical convenience kits labeled as: C-SECTION TRAY-LF, Medline Kit Number/SKU OBN471K

DateOct 22, 2026 (initiated Sep 9, 2026)
StatusOpen, Classified
ReasonReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
Root causeUnder Investigation by firm
ActionMEDLINE issued a MEDICAL DEVICE CORRECTION notice to its consignees on 9/9/2023 via US mail and email. The notice explained the issue and circumstances under which it can occur, hazard involved, and requested the user follow specific patient skin preparation, product application considerations, and removal recommendations. For questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.
Quantity108 kits
DistributionWorldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.