International safety notice
Recall of GlideScope Reusable GVL and AVL Blades, Verathon Inc. / VERATHON MEDICAL (EUROPE) B.V.
Germany / BfArM · DEU · Feb 12, 2016
Key facts
| Title | Recall of GlideScope Reusable GVL and AVL Blades, Verathon Inc. / VERATHON MEDICAL (EUROPE) B.V. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of GlideScope Reusable GVL and AVL Blades, Verathon Inc. / VERATHON MEDICAL (EUROPE) B.V. |
| Manufacturer | Recall of GlideScope Reusable GVL and AVL Blades, Verathon Inc. / VERATHON MEDICAL (EUROPE) B.V. |
| Models | LG152232, 0574-0007, 31.30.68.70.512, 31.30.68.70.512E-MAIL, 0574-0001, AF151525, 31.30.68.70.570, 800.331.2313, AD151535, MD151685, 98011, 0574-0116 and 16 more |
| Date | Feb 12, 2016 |
| 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