International safety notice
Recall of ENDOPATH ETS Compact Flex 45 mm (240 shaft length) articulating linear cutters and Rectal Prolapse Resection Procedure Pack, Ethicon Endo-Surgery
Germany / BfArM · DEU · Aug 22, 2011
Key facts
| Title | Recall of ENDOPATH ETS Compact Flex 45 mm (240 shaft length) articulating linear cutters and Rectal Prolapse Resection Procedure Pack, Ethicon Endo-Surgery |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of ENDOPATH ETS Compact Flex 45 mm (240 shaft length) articulating linear cutters and Rectal Prolapse Resection Procedure Pack, Ethicon Endo-Surgery |
| Manufacturer | Recall of ENDOPATH ETS Compact Flex 45 mm (240 shaft length) articulating linear cutters and Rectal Prolapse Resection Procedure Pack, Ethicon Endo-Surgery |
| Models | AUG-2015, G4RP7N, G4UC07, APR-2016, 75545, H43303, H43F6N, 76501, 74625, 78936, G4RY2D, G4RD0F and 370 more |
| Date | Aug 22, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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