FDA Device recall Z-0231-2024
BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid
- FDA Device
- Class II
- ongoing
- Published 2023-11-15
On 2023-11-15 the FDA classified a Class II recall of BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid by Breg, citing due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0231-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-13 |
| Published | 2023-11-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Breg |
| Distribution | AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WY |
Product
BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.
Reason
Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
Identifiers
| code_info | Model/Product Number - 100519-000 UDI-DI Code: 00672736130834 Lot Numbers: CM82293623, CM82293923, CM82293823, CM824429…Model/Product Number - 100519-000 UDI-DI Code: 00672736130834 Lot Numbers: CM82293623, CM82293923, CM82293823, CM82442923, CM82457323, CM82457423, CM82442823, CM82457523, CM82531023, CM82531223 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0231-2024%22
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