International safety notice
Recall of all Power Medical Interventions, Inc. Products, Covidien
Germany / BfArM · DEU · Oct 26, 2009
Key facts
| Title | Recall of all Power Medical Interventions, Inc. Products, Covidien |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of all Power Medical Interventions, Inc. Products, Covidien |
| Manufacturer | Recall of all Power Medical Interventions, Inc. Products, Covidien |
| Models | LER21, RALC30V, PLCR60G, PES200RC, SLC55B, IR60G, FS3SCG, 267-775-8123, RALC30, I60SRC, FS214RC, 1-866-769-3763 and 29 more |
| Date | Oct 26, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
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