Class II — Breg Inc
| Recalling firm | Breg Inc |
|---|---|
| Registered facility | View this company's 4 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels. |
| Product | BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid. |
| Quantity | 11,193 units |
| Distribution | U.S.: 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, and WY. O.U.S.: N/A |
| Initiated | 2023-09-13 |
| Classified | 2023-11-03 |
| Recall number | Z-0231-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Breg Inc (Z-0231-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93114/
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