International safety notice
Corrective action of Abbott for FreeStyle™, Freestyle Mini™, Precision Xtra™ and Precision Xceed™ blood glucometers
Germany / BfArM · DEU · Jul 27, 2005
Key facts
| Title | Corrective action of Abbott for FreeStyle™, Freestyle Mini™, Precision Xtra™ and Precision Xceed™ blood glucometers |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | FreeStyle™, Freestyle Mini™, Precision Xtra™ and Precision Xceed™ blood glucometers |
| Manufacturer | Corrective action of Abbott for FreeStyle™, Freestyle Mini™, Precision Xtra™ and Precision Xceed™ blood glucometers |
| Models | 1084565, 0677808, 1075425, 0677814, 0352182, 65205, 1075454, 1075448, 65003, 1084513, 1510648, 1084453 and 9 more |
| Date | Jul 27, 2005 |
| 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