Belle Isle, FL, United States
Acorn Stairlifts, Inc recalls
1 recall recorded since 2018, most recently on 20 April 2016. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 20 April 2016
- Reason
- The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.
- Distribution
- Distributed nationwide to AL, AK, AZ, AR, CA, CO, CT, DE, DC, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, VI, WA, WV, WI, and WY, as well as Puerto Rico and the Virgin Islands. There was no
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0681-2022
- Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.