MediBeads King Pad — Class II medical device recall Z-1367-2024
Ongoing recall by Bruder Healthcare Company, LLC, reported 2024-04-03, distributed nationwide. Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, r
| Recall number | Z-1367-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bruder Healthcare Company, LLC, Alpharetta, GA, United States |
| Recall initiated | 2024-02-21 |
| Classified | 2024-03-22 |
| Reported by FDA | 2024-04-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 585 units |
| Reason classes | microbial contamination |
| Pathogens | mold |
| UPC / GTIN / UDI-DI | 00041533341208 |
| Lot numbers | M053280, M053590 |
| Model numbers | 34120, 34120PM, 34125R |
Product
MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R
Reason for recall
Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
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-1367-2024. 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.