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Action®
ACTION PRODUCTS, INC. · Model Wheelchair Back Rest · UDI-DI 00089904008244
2
510(k) clearances
134
Adverse events (1 deaths)
1
Recalls
171
Facilities
Description
Twister® Adaptive Back 1718 - Short
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-01-31 | Bock,Otto,Orthopedic Ind,Inc | 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 fl |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
