Recall Z-0681-2022— Acorn Stairlifts, Inc
Class II · Ongoing
Class II FDA medical device recall by Acorn Stairlifts, Inc, initiated 2016-04-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift. Reason: The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use..
- Recalling firm
- Acorn Stairlifts, Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2016-04-20
- Firm location
- Belle Isle, FL, United States
Product description
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Reason for recall
The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.
Data sourced from openFDA. This site is unofficial and independent of the FDA.