FDA recall Z-0681-2022

Acorn Stairlifts, Inc · Class II · device

Product

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.

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 foreign/military/government distribution.

Key facts

Status
Ongoing
Initiation date
2016-04-20
Report date
2022-03-09
Voluntary/Mandated
Voluntary: Firm initiated
Location
Belle Isle, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0681-2022