Breg Inc: Medical Device Recall in 2023 - (Recall #: Z-0231-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 13, 2023

Date Posted: November 15, 2023

Recall Number: Z-0231-2024

Event ID: 93114

Reason for Recall:

Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.

Status: Ongoing

Product Quantity: 11,193 units

Code Information:

Model/Product Number - 100519-000 UDI-DI Code: 00672736130834 Lot Numbers: CM82293623, CM82293923, CM82293823, CM82442923, CM82457323, CM82457423, CM82442823, CM82457523, CM82531023, CM82531223

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated