TemporaryFDAOngoing
Can cause harm that is usually temporary.
MEDLINE medical convenience kits labeled as: 1) FETAL SURGERY CDS-LF, Medline Kit Number/SKUCDS840214R; 2) MAJOR, Medline Kit Number/SKUDYNJ904851I; 3) ABDOMINAL TRANSPLANT, Medline Kit Number/SKUDYNJ908124B.
Check the device or its packaging for
Medline Product Number/SKU DYNJP6101, UDI/DI 10198459447594 (each) 40198459447595 (case), Lot Number 26GBC179, Medline Product Number/SKU DYNJP6101, UDI/DI 10198459217623 (each) 40198459217624 (case), Lot Number 26HBV769, Medline Product Number/SKU DYNJP6101, UDI/DI 10198459217623 (each) 40198459217624 (case), Lot Number 26GBJ833, Medline Product Number/SKU DYNJP6101, UDI/DI 10198459217623 (each) 40198459217624 (case), Lot Number 26EBT593, Medline Product Number/SKU DYNJP6106, UDI/DI 10198459012648 (each) 40198459012649 (case), Lot Number 26DLB020, Medline Product Number/SKU DYNJP6108, UDI/DI 10198459012648 (each) 40198459012649 (case), Lot Number 26DLA431, Medline Product Number/SKU DYNJP6108, UDI/DI 10198459012648 (each) 40198459012649 (case), Lot Number 26BLA251.
- 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-0274-2027 · retrieved 22 October 2026
Read the official notice