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MANOMETER
Pajunk GmbH Medizintechnologie · Model 001163-38F · UDI-DI 04048223049860
1
510(k) clearances
411
Adverse events (1 deaths)
5
Recalls
11
Facilities
Description
001163-38F
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-02-22 | Busse Hospital Disposables, Inc. | Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to unce |
| 2004-09-09 | Smiths Medical ASD, Inc. | Sterility of the device is compromised due to packaging defects |
| 2004-09-09 | Smiths Medical ASD, Inc. | Sterility of the device is compromised due to packaging defects |
| 2004-09-09 | Smiths Medical ASD, Inc. | Sterility of the device is compromised due to packaging defects |
| 2004-09-09 | Smiths Medical ASD, Inc. | Sterility of the device is compromised due to packaging defects |
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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.