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n.a.
VBM Medizintechnik GmbH · Model 88-11-000 · UDI-DI 14250105628507
BYW
Prescription
2
510(k) clearances
29
Adverse events
1
Recalls
31
Facilities
Description
Small Infant Mask
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-10-31 | Teleflex Medical | Mislabeling-The rebreathing bag is incorrectly labeled as a 1 liter bag when it is actually a 1/2 liter bag. |
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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.