International safety notice
Boston Scientific recalls Enteryx Procedure Kits and Enteryx Injector products
Germany / BfArM · DEU · Oct 14, 2005
Key facts
| Title | Boston Scientific recalls Enteryx Procedure Kits and Enteryx Injector products |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Boston Scientific recalls Enteryx Procedure Kits and Enteryx Injector products |
| Manufacturer | Boston Scientific recalls Enteryx Procedure Kits and Enteryx Injector products |
| Models | M00572600, EF010712, 72103, FCA2005-31, 52003, 713532B, 40611, 50318, 50211, 489OOF, 489AOF, 31215 and 110 more |
| Date | Oct 14, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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