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Composite Respiratory Kit- Medical West
WESTMED, INC. · Model 0713 · UDI-DI 00709078003608
0
510(k) clearances
13
Adverse events
1
Recalls
15
Facilities
Description
2 - Packaged 25' O2 Tubing (0025), 6 - Packaged Soft Cannula with 7' Tubing (0556), 1 - Swivel Connector (0590), 1 - Barbed Connector (40076).
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-10-17 | Vital Signs Devices, a GE Healthcare Company | Povidone Iodine Pads included in the Vital Signs Broselow Pediatric Emergency Kit may be contaminated with Elizabethkinga meningoseptica. |
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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.
