Acorn 180 Curved Stairlift
FDA Recall Z-1530-2016 · Posted None
Recalling FirmAcorn Stairlifts Inc
Recall StatusTerminated
Product CodePCD
Date Initiated2016-02-17
Date Terminated2019-01-29
Product Quantity1,290 USA and 9,607 Foreign
Reason for Recall
Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
Firm Action
Customers were notified by phone calls, documents mailed with a Rationalization Action plan to follow. Contact information 1-888-563-0410 x1500 or 1400
Root Cause
Component change control
Distribution Pattern
Worldwide Distribution - USA (nationwide) Distribution to the states of : AL, AZ, CA, CO, DE, FL, GA, IL, IN, KS, KY, LA, MA, ME, MD, MI, MO, NH, NJ, NY, NC, OH, PA, RI, SC, TN, TX, UT, VT, VI, WA, WV, WI, and District of Columbia and to the countries of UK and Germany.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.