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Aerobika,OPEP
Monaghan Medical Corporation · Model Aerobika, OPEP Device, Retail · UDI-DI 00604351505124
BWF
Prescription
1
510(k) clearances
182
Adverse events (4 deaths)
1
Recalls
53
Facilities
Description
AEROBIKA, OPEP DEVICE, RETAIL- 50512
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-12-21 | Smiths Medical ASD Inc. | Shipping box may contain wrong model. |
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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.