Z-1530-2016 Class II Terminated
FDA device recall Z-1530-2016 was initiated by Acorn Stairlifts Inc on February 17, 2016 and is designated Class II. Reason for recall: Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break. The recall status is terminated (terminated January 29, 2019). Affected quantity: 1,290 USA and 9,607 Foreign.
Recall Details
- Product Type
- Devices
- Report Date
- April 27, 2016
- Initiation Date
- February 17, 2016
- Termination Date
- January 29, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,290 USA and 9,607 Foreign
Product Description
Acorn 180 Curved Stairlift
Reason for Recall
Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
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.
Code Information
Serial Numbers: 140401487591 to 140410249946. All models manufactured before April 2012