Recall Z-0275-2027— 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 medical convenience kits labeled as (list truncated). 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 medical convenience kits labeled as (list truncated)
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.