Data Foundry

Medical device recalls 2013

Invacare Power Wheelchair — Class II medical device recall Z-2270-2013

Terminated recall by Invacare Corporation, reported 2013-10-02, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Unintended slowing or deceleration, and on rare occasion, unanticipated and unattended acceleration of power w

Recall numberZ-2270-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmInvacare Corporation, Elyria, OH, United States
Recall initiated2013-06-04
Classified2013-09-23
Reported by FDA2013-10-02
Terminated2016-01-04
DistributedAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY
Countries outside the USAU, BM, BR, CA, CN, CR, DE, FR, GB, HK, IL, IN, KW, NZ, QA, SA, SG, TH, TT, ZA
Quantity166,230

Product

Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.

Reason for recall

Unintended slowing or deceleration, and on rare occasion, unanticipated and unattended acceleration of power wheelchairs equipped with SPJ and MPJ type joysticks.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2270-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.