International safety notice
Recall for certain lots of 9Fr ACUITY Pro Coronary Sinus Outer Guide Catheters, Boston Scientific
Germany / BfArM · DEU · Dec 11, 2015
Key facts
| Title | Recall for certain lots of 9Fr ACUITY Pro Coronary Sinus Outer Guide Catheters, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | certain lots of 9Fr ACUITY Pro Coronary Sinus Outer Guide Catheters, Boston Scientific |
| Manufacturer | Recall for certain lots of 9Fr ACUITY Pro Coronary Sinus Outer Guide Catheters, Boston Scientific |
| Models | 18437680, 18421013, 18408497, 18410783, 18288704, 18284604, 18324876, 18477470, 18286265, 18371973, 18332118, 18330946 and 138 more |
| Date | Dec 11, 2015 |
| 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