Z-0212-05

Lift Chairs. Electric Positioning Chair

Name: Z-0212-05 Lift Chairs. Electric Positioning Chair
Creator: Pride Mobility Products Corp
Published: 2004-06-07
License: https://open.fda.gov/license/

Pride Mobility Products Corp / initiated 2004-06-07 / Terminated

FDA source

Pride Mobility Products Corp began a recall of Lift Chairs. Electric Positioning Chair on 2004-06-07. The reason FDA records is "The heating pad on these Lift Chairs may tear at the entry point causing a short and/or overheating, which can damage the chair". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0212-05
Status: Terminated
Initiated: 2004-06-07
Posted: 2004-11-19
Terminated: 2006-08-10
Recalling firm: Pride Mobility Products Corp
Product: Lift Chairs. Electric Positioning Chair.
Product code: INO Chair, Positioning, Electric
Reason for recall: The heating pad on these Lift Chairs may tear at the entry point causing a short and/or overheating, which can damage the chair.
FDA 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 in commerce: 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.
Product codes and lots: Model Numbers: C20, C30, GL358S, GL358L, TMR58, TMR540, TMR560, TMR570T, TMR571, TMR585, DMR670, TMR805, and TMR450.

Product code INO

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)