RecallRadar

FDA Device recall Z-0231-2024

BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid

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

AgencyFDA Device
Recall numberZ-0231-2024
ClassificationClass II
Statusongoing
Initiated2023-09-13
Published2023-11-15
Last updated2026-09-13 11:56 UTC
CompanyBreg
DistributionAL, 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

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.