FDA Medical Device Recalls (openFDA)
Acorn Stairlifts Inc: Acorn 180 Curved Stairlift
- Recall number
- Z-1530-2016
- Recalling firm
- Acorn Stairlifts Inc
- Product
- Acorn 180 Curved Stairlift
- Status
- Terminated
- Initiated
- 2016-02-17
- Posted
- not on file
- Terminated
- 2019-01-29
- Reason
- Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
- Root cause
- Component change control
- 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
- Quantity
- 1,290 USA and 9,607 Foreign
- Distribution
- 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.
- Lot, serial or model codes
- Serial Numbers: 140401487591 to 140410249946. All models manufactured before April 2012
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- PCD
- Firm FEI
- 3003124453
- Firm city
- Orlando
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28