TemporaryFDAOngoing
Can cause harm that is usually temporary.
MEDLINE medical convenience kits labeled as: 1) LAPAROTOMY GYN CDS, Medline Kit Number/SKU CDS983529O; 2) GYN ROBOTIC PK-LF, Medline Kit Number/SKU DYNJ52432M; 3) TAH PACK, Medline Kit Number/SKU DYNJ60646A; 4) TUBAL LIGATION RFD, Medline Kit Number/SKU DYNJ906291F.
Check the device or its packaging for
Medline kit number/SKU CDS983529O, UDI/DI 10198459603464 (each) 40198459603465 (case), Lot Number CDS983529O; Medline kit number/SKU CDS983529O, UDI/DI 10198459603464 (each) 40198459603465 (case), Lot Number CDS983529O; Medline kit number/SKU DYNJ52432M, UDI/DI 10198459508035 (each) 40198459508036 (case), Lot Number DYNJ52432M; Medline kit number/SKU DYNJ52432M, UDI/DI 10198459508035 (each) 40198459508036 (case), Lot Number DYNJ52432M; Medline kit number/SKU DYNJ60646A, UDI/DI 10198459363658 (each) 40198459363659 (case), Lot Number DYNJ60646A; Medline kit number/SKU DYNJ60646A, UDI/DI 10198459363658 (each) 40198459363659 (case), Lot Number DYNJ60646A; Medline kit number/SKU DYNJ906291F, UDI/DI 10198459419591 (each) 40198459419592 (case), Lot Number DYNJ906291F; Medline kit number/SKU DYNJ906291F, UDI/DI 10198459419591 (each) 40198459419592 (case), Lot Number DYNJ906291F.
- Why
- Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
- Distributed
- Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.
- Company
- Medline Industries, LP
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-0277-2027 · retrieved 22 October 2026
Read the official notice