Recall Z-0231-2024— Breg Inc
Class II · Ongoing
Class II FDA medical device recall by Breg Inc, initiated 2023-09-13. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Breg Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-09-13
- Firm location
- Carlsbad, CA, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.