FDA Device recall Z-1367-2024
MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R
- FDA Device
- Class II
- ongoing
- Published 2024-04-03
On 2024-04-03 the FDA classified a Class II recall of MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R by Bruder Healthcare, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1367-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-21 |
| Published | 2024-04-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Bruder Healthcare |
| Distribution | US |
Product
MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R
Reason
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.
Identifiers
| upc | 041533341208 |
|---|---|
| code_info | UPC 041533341208, Lot Numbers: M053590, M053280 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1367-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.