Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Check against the official notice below — it lists the full affected range.
Acorn Stairlifts, Inc. is recalling approximately 26,428 units of Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift models because the seat design does not consistently provide adequate strength to support customers' weight with continued use. The affected stairlifts were distributed nationwide across all U.S. states, Puerto Rico, and the Virgin Islands.
The recall applies to specific serial numbers of the Acorn 130/180 Seat Squab component used in Acorn 130 Straight Stairlifts and Acorn 180 Curved Stairlifts. According to the recall record, no remedy information is provided for consumers who own affected units.
Written by software from the official notice below. Not reviewed by a lawyer.
The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.
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. Quantity: 26,428 Lot/code info: Acorn 130/180 Seat Squab, included as part of The Acorn 130 Straight Stairlift and the Acorn 180 Curved Stairlift. Serial Numbers: 140110386215,140110356934,140110330295,140110410265,140110356903,140110319711,140110353380,140110358263,140110387720,140110357449,140110348263,140110380857,140110357022,140110334193,140110390695,140110348564,140110364396,140110362060,140110278902,140110360364,140110263037,140110366547,140110320108,140110372638,140110387248,140110367036,140110311884,140110405234,140110387712,140110400646,140110378178,140110393130,140110389009,140110348935,140110409990,140110413893,140110392454,140110253282,140110406587,140110367992,140110370968,140110367770,140110308838,140110387501,140110402408,140110361497,140110366632,140110365928,140110352238,140110406996,140110401030,140110382733,140110361514,140110363598,140110382800,140110387432,140110367208,140110391181,140110374800,140110370938,140110399914,140110253288,140110355287,140110405166,140110301171,140110358373,140110286761,140110364341,140110399265,140110352528,140110358931,140110358946,140110362374,140110362380,140110366428,140110369259,140110369263,140110369271,140110369300,140110378184,140110378198,140110378199,140110378209,140110382307,140110382320,140110382353,140110399571,140110399585,140110399595,140110402205,140110410470,140110413890,140110413896,140110413899,140110361487,140110361821,140110361829,140110361833,140110361839,140110363852,140110363880,140110363562,140110363564,140110363568,140110363569,1401
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.