Medical device recalls Moderate risk

MEDLINE INDUSTRIES, LP - Northfield recalls Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT, Model Number: MJ18004V2; 2) MJ BANDAGE HYDROCOLLO…

Recall date
February 19, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1531-2025
FDA classification
Class II
Brand / firm
MEDLINE INDUSTRIES, LP - Northfield
Sold / distributed
Worldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of: Bermuda, Canada, Panama, Singapore

Why it was recalled

There is a potential for the sterility of the device to be compromised.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT, Model Number: MJ18004V2; 2) MJ BANDAGE HYDROCOLLOID ALL PURP 10CT, Model Number: MJ18005V2; 3) MJ BNDG HYDROCOLLOID FINGER TOE 8CT, Model Number: MJ76126V2; 4) WALMART,BANDAGE,HYDROCOLLOID,HEEL,6CT, Model Number: WAL1901; 5) WALMART,HYDROCOLLOID,TOE,8CT, Model Number: WAL1902;

Get recall alerts

Free email alert whenever MEDLINE INDUSTRIES, LP - Northfield has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: MEDLINE INDUSTRIES, LP - Northfield