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Stratis®
PHARMAJET, INC. · Model C501-46 · UDI-DI 00856457003336
KZE
Prescription
1
510(k) clearances
467
Adverse events (2 deaths)
1
Recalls
11
Facilities
Description
Stratis® 13mm Vial Adapter
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-06-01 | CaridianBCT, Inc. | Labeling clarification and software updates to include fixes for end of run summaries, increasing boot reliability, corrections to the double red blood cell count collection TBV li |
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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.