Chenica Gunnell Rehab Series of Wheelchairs — Class II medical device recall Z-0809-2013
Completed recall by CHENICA INC., reported 2013-02-20, distributed nationwide. The wheelchairs may not meet the specifications of WC-19 (crash testing), therefore the WC-19 verbiage and cor
| Recall number | Z-0809-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | CHENICA INC., Vassar, MI, United States |
| Recall initiated | 2013-01-18 |
| Classified | 2013-02-13 |
| Reported by FDA | 2013-02-20 |
| Terminated | 2014-04-15 |
| Distributed | Nationwide (US) |
| Quantity | 53 |
| Serial numbers | 36977-1210, 36988-1210, 36999-1210, 37000-1210, 37003-1210, 37014-1210, 37061-0211, 37067-0111, 37094-0211, 37114-0211, 37122-0211, 37137-0311, 37141-0311, 37185-0311, 37194-0312, 37220-0511, 37234-0511, 37273-0611, 37286-0511, 37296-0611, 37305-0711, 37307-0711, 37333-0711, 37348-0811, 37374-0911 and 28 more |
Product
Chenica Gunnell Rehab Series of Wheelchairs (GRSW); Mechanical Wheelchair, Sold as Rehab Tough and Tilt (TNT), Rehab Recline and Mobility (RAM), Rehab Kidster (Kidster). Provide mobility to individuals limited to a seating position.
Reason for recall
The wheelchairs may not meet the specifications of WC-19 (crash testing), therefore the WC-19 verbiage and corresponding logo are removed from the flyers on the Gunnell Rehab Series of Wheelchairs (GRSW).
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-0809-2013. 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.