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Spectrum, Inc.
SPECTRUM, INC. · Model 985-03514-000 · UDI-DI 00855495007269
FQL
Prescription
6
510(k) clearances
24
Adverse events
2
Recalls
272
Facilities
Description
1 Ply Stockinette- 50/50% - 4" X 3 Yards - Sterile
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-10-07 | Surgical Appliance Industries | During an audit with the FDA, it was discovered that a new compression testing device used for testing hosiery had been implemented and that the operators were not properly trained |
| 2011-10-07 | Surgical Appliance Industries | During an audit with the FDA, it was discovered that a new compression testing device used for testing hosiery had been implemented and that the operators were not properly trained |
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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.