Recall Z-0270-2027— Medline Industries, LP
Class II · Ongoing
Class II FDA medical device recall by Medline Industries, LP, initiated 2026-09-09. FDA's recall record names no specific 510(k) clearance for this event. Product: MEDLINE DRAPE C-SEC FEN CLEAR SCRN WIRE, Medline Product Number/SKU DYNJP6106. Reason: Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin..
- Recalling firm
- Medline Industries, LP
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-09-09
- Firm location
- Northfield, IL, United States
Product description
MEDLINE DRAPE C-SEC FEN CLEAR SCRN WIRE, Medline Product Number/SKU DYNJP6106
Reason for recall
Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
Data sourced from openFDA. This site is unofficial and independent of the FDA.