MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD recall (Medline Industries, LP)
Medical deviceClass IIOngoing
Summary: Medline Industries, LP is recalling MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD, Medline Product Number/SKU DYNJ906291G. Reason: Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
What is being recalled
MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD, Medline Product Number/SKU DYNJ906291G
Why
Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE. (states named: California)
How to tell if yours is affected
UDI/DI 10198459847752 (each) 40198459847753 (case), Lot numbers: 26GBQ124
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-0279-2027 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | September 9, 2026 |
| Reported | October 28, 2026 |
| Company | Medline Industries, LP |
| Company location | Northfield, IL, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 3 kits |
More recalls from Medline Industries, LP · all medical device recalls · recalls from September 2026