FDA Medical Device Recalls (openFDA)
Pride Mobility Products Corp: Lift Chairs. Electric Positioning Chair.
- Recall number
- Z-0212-05
- Recalling firm
- Pride Mobility Products Corp
- Product
- Lift Chairs. Electric Positioning Chair.
- Status
- Terminated
- Initiated
- 2004-06-07
- Posted
- 2004-11-19
- Terminated
- 2006-08-10
- Reason
- The heating pad on these Lift Chairs may tear at the entry point causing a short and/or overheating, which can damage the chair.
- Root cause
- Other
- Action
- The recalling firm sent a Safety Alert notification to their direct accounts on 5/14/04 informing them of the problem. The direct accounts were instructed to locate the end user and inform them of the problem. Once the chair has been located the direct account is to contact the recalling firm for a replacement and return the recalled chair.
- Quantity
- 532 units
- Distribution
- The recalled product was distributed through dealers nationwide. The affected states are as follows: AL, AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, OH, OK, MA, MD, MI, MN, MO,MS, NC, ND, NE, NH, NJ, NM, NV, NY, PA, SC, TN, TX, UT, VA, VT, WA, and WV . There is one government account in FL.
- Lot, serial or model codes
- Model Numbers: C20, C30, GL358S, GL358L, TMR58, TMR540, TMR560, TMR570T, TMR571, TMR585, DMR670, TMR805, and TMR450.
- 510(k) numbers
- ["K821827","K852864","K931349","K953342"]
- PMA numbers
- not on file
- Product code
- INO
- Firm FEI
- not on file
- Firm city
- Exeter
- Firm state
- PA
- 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