FDA Device recall Z-1366-2024
MediBeads Neck Wrap, Item Number 34320
- FDA Device
- Class II
- ongoing
- Published 2024-04-03
On 2024-04-03 the FDA classified a Class II recall of MediBeads Neck Wrap, Item Number 34320 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-1366-2024 |
| 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 Neck Wrap, Item Number 34320
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 | 041533343202 |
|---|---|
| code_info | UPC 041533343202, Lot Numbers: M053300 |
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-1366-2024%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.