International safety notice
Incorrect Instructions for Use with the Model 93600 of the Closed Injectate Delivery Systems from Edwards Lifesciences
Germany / BfArM · DEU · Apr 3, 2007
Key facts
| Title | Incorrect Instructions for Use with the Model 93600 of the Closed Injectate Delivery Systems from Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Use with the Model 93600 of the Closed Injectate Delivery Systems from Edwards Lifesciences |
| Manufacturer | Incorrect Instructions for Use with the Model 93600 of the Closed Injectate Delivery Systems from Edwards Lifesciences |
| Models | 58237308, 116H0634, 42443278, 116D072C, 146J0720T, 8226337, F16HC.634, ÖG0575E, 9ZÆOO, 16K0939 |
| Date | Apr 3, 2007 |
| 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