Wayson Hydrocolloid Models: 1) Model Number: CUR5103 — Class II medical device recall Z-1530-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-04-16, distributed nationwide. There is a potential for the sterility of the device to be compromised.
| Recall number | Z-1530-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2025-02-19 |
| Classified | 2025-04-04 |
| Reported by FDA | 2025-04-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | BM, CA, PA, SG |
| Quantity | 364,842 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00011822538183, 00708820502734, 00708820656963, 00708820656970, 00888277307400, 20708820656967, 20708820656974, 40011822538181, 40708820502732, 40888277307408 |
| Lot numbers | 100, 101, 102, 103, 10315040001, 10317020005, 10317030004, 10317120001, 10318050003, 10318070002, 10318080003, 10319010004, 10319020001, 10319050003, 10319050004, 10319050005, 10319060001, 10319070003, 10319080001, 10319080003, 10319080004, 10319100004, 10319110001, 10319110002, 10319110004, 10319120001, 10319120004, 10320030003, 10320030005, 10320040002, 10320050002, 10320070001, 10320070003, 10320080001, 10320080002, 10320090001, 10320090003, 10320090004, 10320100001, 10320100002 and 96 more |
| Model numbers | CUR5103, MJ18004, MJ18005, MJ76126V1, RA0353818V1 |
Product
Wayson Hydrocolloid Models: 1) Model Number: CUR5103, DBD-BNDG,WTRPRF,HYDRCLLD,CLR,2.36X3.93", 2) Model Number: MJ18004, DBD-MEIJER,BANDAGE,HYDROCOLLOID,HEEL,OVL 3) Model Number: MJ18005, MEIJER,BANDAGE,HYDROCOLLOID,ALLPURP,10CT 4) Model Number: MJ76126V1, DBD-MEIJER,HYDROCOLLOID,FINGER&TOE,8CT 5) Model Number: RA0353818V1, BANDAGE,BLISTER, RITEAID,6EA/BX, 24BX/CS
Reason for recall
There is a potential for the sterility of the device to be compromised.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1530-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.