Otto Bock Aerial and Aerial Active Wheelchair Cushions — Class II medical device recall Z-1266-2014
Terminated recall by Bock,Otto,Orthopedic Ind,Inc, reported 2014-03-26, distributed nationwide. Otto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from specific material numbers. During
| Recall number | Z-1266-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bock,Otto,Orthopedic Ind,Inc, Minneapolis, MN, United States |
| Recall initiated | 2014-01-31 |
| Classified | 2014-03-20 |
| Reported by FDA | 2014-03-26 |
| Terminated | 2018-05-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BR, CH, CN, DE, DK, ES, FR, GB, GR, HK, HR, HU, IS, JP, MX, NL, PL, RO, RU, SE, TH, ZA |
Product
Otto Bock Aerial and Aerial Active Wheelchair Cushions. Material numbers: SK757 476C00=SK701, 476C00=SK702, 476C00=SK703, 476C00=SK704, 476C00=SK705, 476C00=SK706, 476C00=SK707, The following material numbers were not distributed within the US: 476C00=SK751, 476C00=SK752, 476C00=SK753, 476C00=SK754, 476C00=SK755, 476C00=SK756, 476C00= SK757.
Reason for recall
Otto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from specific material numbers. During internal testing, it was discovered that there is a small risk of flammability to the cushion after it has been washed at high temperatures. The cushions should either be returned to Otto Bock or destroyed.
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-1266-2014. 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.