International safety notice
Lot recall of Inflation device REF 2080-9030020 LOT 1210127, Spiggle & Theis Medizintechnik GmbH
Germany / BfArM · DEU · Nov 6, 2013
Key facts
| Title | Lot recall of Inflation device REF 2080-9030020 LOT 1210127, Spiggle & Theis Medizintechnik GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of Inflation device REF 2080-9030020 LOT 1210127, Spiggle & Theis Medizintechnik GmbH |
| Manufacturer | Lot recall of Inflation device REF 2080-9030020 LOT 1210127, Spiggle & Theis Medizintechnik GmbH |
| Models | 12101273, 2080-9030020, 9030020 |
| Date | Nov 6, 2013 |
| 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