- 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 Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26FBB857; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26EBA908; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26CBV797; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26ABM708; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 25KBQ582; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26GBV395; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26FBO061; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26DBF331; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26BBT983; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 25LBJ546; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 25KBK623; Medline Kit Number/SKU DYNJ911652, UDI/DI 10198459481673 (each) 40198459481674 (case), Lot Number 26DME349.
- Units affected
- 2229 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-0276-2027
- 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
