BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a… — Class II medical device recall Z-0231-2024
Ongoing recall by Breg Inc, reported 2023-11-15, distributed in AL, AR, AZ, CA, CO, CT, FL, GA…. Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
| Recall number | Z-0231-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Breg Inc, Carlsbad, CA, United States |
| Recall initiated | 2023-09-13 |
| Classified | 2023-11-03 |
| Reported by FDA | 2023-11-15 |
| Distributed | 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 |
| Quantity | 11,193 units |
| UPC / GTIN / UDI-DI | 00672736130834 |
| Lot numbers | CM82293623, CM82293823, CM82293923, CM82442823, CM82442923, CM82457323, CM82457423, CM82457523, CM82531023, CM82531223 |
| Model numbers | 100519-000 |
Product
BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.
Reason for recall
Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
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-0231-2024. 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.