Home › SPEX LIMITED › Spex Limited
Spex Limited
SPEX LIMITED · Model 1102-1416-WSS_054 · UDI-DI 09420082697232
2
510(k) clearances
134
Adverse events (1 deaths)
1
Recalls
171
Facilities
Description
Wonderseat Cushion, 14" Wide x 16" Deep, SuperHigh Contour - Leaf Green
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 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.