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;
FDA Recall Z-1531-2025 · Posted 2025-04-04
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Recalling FirmMEDLINE INDUSTRIES, LP - Northfield
Recall StatusOpen, Classified
Product CodeNAD
Date Initiated2025-02-19
Product Quantity1894488 units
Reason for Recall
There is a potential for the sterility of the device to be compromised.
Firm Action
An "URGENT MEDICAL DEVICE RECALL" notification letter dated 2/19/25 was sent to customers.
REQUIRED ACTION:
1.Immediately check your stock for the affected item number and the affected lot numbers which can be located within the recall portal.
2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form.
3.Please destroy any affected inventory. Medline will issue credit for the product based upon the quantity and lot numbers identified on the submitted response form
The login for completing the response form is: Website link: https://recalls.medline.com Recall Reference #: R-25-026 Recall Code: Recall Code
4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers document and destroy any affected product, and include your customer s quantities on your response form.
If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of: Bermuda, Canada, Panama, Singapore
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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