Z-0303-06

3G Storm Series Power Wheelchair with Power Tilt Option

Name: Z-0303-06 3G Storm Series Power Wheelchair with Power Tilt Option
Creator: Invacare Corporation
Published: 2005-10-11
License: https://open.fda.gov/license/

Invacare GmbH / initiated 2005-10-11 / Terminated

FDA source

Invacare Corporation began a recall of 3G Storm Series Power Wheelchair with Power Tilt Option on 2005-10-11. The reason FDA records is "When the powered seating system is tilted completely in the rearward position, a potential pinch point is created between the seat and the seat frame". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0303-06
Status: Terminated
Initiated: 2005-10-11
Posted: 2005-12-23
Terminated: 2012-04-12
Recalling firm: Invacare GmbH
Product: 3G Storm Series Power Wheelchair with Power Tilt Option.
Product code: ITI Wheelchair, Powered
Reason for recall: When the powered seating system is tilted completely in the rearward position, a potential pinch point is created between the seat and the seat frame.
FDA root cause: Other
Action: The recalling firm sent letters to all consignees.
Quantity in commerce: 16 devices
Distribution: The product was sent to distributors located in AL, GA, CA, IL, KS, MN, NC, PA, TX, and VA.
Product codes and lots: Serial numbers: 05G066858, 05G066859, 05G071801, 05G071803, 05G077773, 05G079666, 05G089011, 05G089012, 05G092274, 05G105434, 05G106984, 05G111332, 05G117359, 05G121857, 05G125563, 05H144898

Product code ITI

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)