FDA Device Intelligence
Home › WESTMED, INC. › Composite Respiratory Kit: Performance Home Medical

Composite Respiratory Kit: Performance Home Medical

WESTMED, INC. · Model 0836 · UDI-DI 00709078002540

OGLBYXCAT Prescription
0
510(k) clearances
13
Adverse events
1
Recalls
15
Facilities

Description

Composite Respiratory Kit: Performance Home Medical 2-0194B, 2-0556B, 1-0027B, 1-0052B, 1-No Smoking Sign, 2-0590B

Recalls

DateFirmReason
2011-10-17Vital Signs Devices, a GE Healthcare CompanyPovidone Iodine Pads included in the Vital Signs Broselow Pediatric Emergency Kit may be contaminated with Elizabethkinga meningoseptica.

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 docs
Data 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.