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PAD 1110
Tz Medical, Inc. · Model PAD 1110 · UDI-DI 00811331017779
1
510(k) clearances
599
Adverse events (19 deaths)
22
Recalls
23
Facilities
Description
CABLE - LIFEPAK 10 OR 12
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
| 2020-03-10 | Smiths Medical ASD Inc. | Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets. |
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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.