- Recalling firm
- Medline Industries, LP
- Reason for recall
- Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
- Affected products (lot / model / serial)
- 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.
- Units affected
- 233 kits
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-0274-2027
- Recall initiated
- September 9, 2026
- FDA classification date
- October 22, 2026
- FDA report date
- October 28, 2026
- FDA event ID
- 99960
- Last updated on HTM Vibe
- November 3, 2026
