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PEP
PARI RESPIRATORY EQUIPMENT, INC. · Model 044B4612 · UDI-DI 00744229440383
BWF
Prescription
10
510(k) clearances
182
Adverse events (4 deaths)
1
Recalls
52
Facilities
Description
Monitor Set, PEP, w/Hose, DHD
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-12-21 | Smiths Medical ASD Inc. | Shipping box may contain wrong model. |
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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.
