International safety notice
Lot recall of Covidien Curity All Purpose Gauze Sponges / Curity X-Ray Detectable Laparotomy Sponges / Kerlix X-Ray Detectable Laparotomy Sponges and Vistec X-Ray Detectable Sponges, Medtronic
Germany / BfArM · DEU · Apr 4, 2016
Key facts
| Title | Lot recall of Covidien Curity All Purpose Gauze Sponges / Curity X-Ray Detectable Laparotomy Sponges / Kerlix X-Ray Detectable Laparotomy Sponges and Vistec X-Ray Detectable Sponges, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of Covidien Curity All Purpose Gauze Sponges / Curity X-Ray Detectable Laparotomy Sponges / Kerlix X-Ray Detectable Laparotomy Sponges and Vistec X-Ray Detectable Sponges, Medtronic |
| Manufacturer | Lot recall of Covidien Curity All Purpose Gauze Sponges / Curity X-Ray Detectable Laparotomy Sponges / Kerlix X-Ray Detectable Laparotomy Sponges and Vistec X-Ray Detectable Sponges, Medtronic |
| Models | 959-304, 100000009962, 110000463762, 130002191062X, 110000142862, 15J070162X, 110000161662, 110000476162, 100000010062, 120002259962, 15J163262X, 110001358162 and 20 more |
| Date | Apr 4, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1