International safety notice
Recall of Covidien Devon Light Gloves and non-sterile sub assembly kits, Medtronic
Germany / BfArM · DEU · Jan 25, 2017
Key facts
| Title | Recall of Covidien Devon Light Gloves and non-sterile sub assembly kits, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Covidien Devon Light Gloves and non-sterile sub assembly kits, Medtronic |
| Manufacturer | Recall of Covidien Devon Light Gloves and non-sterile sub assembly kits, Medtronic |
| Models | 31141784, 02634, 571711, EC067893, K-1960-S, 31140257, 99-XXXX, WESTERWALDSTR.4, NS-3600-B, 06473, D-56579, 31140216 and 2 more |
| Date | Jan 25, 2017 |
| 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