- 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)
- UDI/DI 10080196913589 (each) 40080196913580 (case), Lot numbers: 31124090032F, 31125080028F, 31126050023F, 31126060021F.
- Units affected
- 4765 units
- 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-0269-2027
- 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
