FDA Device recall Z-0055-2021
Quick Release Gait Belt, 60
- FDA Device
- Class II
- ongoing
- Published 2020-10-14
On 2020-10-14 the FDA classified a Class II recall of Quick Release Gait Belt, 60 by Medline Industries, citing the buckle on the Gait Belt may break due to degradation of the material due to exposure to gamma radiation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0055-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-09-15 |
| Published | 2020-10-14 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medline Industries |
| Distribution | IL, MI |
Product
Quick Release Gait Belt, 60
Reason
The buckle on the Gait Belt may break due to degradation of the material due to exposure to gamma radiation.
Identifiers
| code_info | Model: MDT821208NATM /503689 Lots: 33019040001, 33019090001 and 33019100001 Used in kits with model number: DYKF1045 Lots: 20EBB832 and 20EBM643. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0055-2021%22
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