International safety notice
Lot recall for GlideScope Video Laryngoscope Titanium Single-Use (SU) Blades, Verathon Incorporated / VERATHON MEDICAL (EUROPE) B.V.
Germany / BfArM · DEU · Mar 22, 2016
Key facts
| Title | Lot recall for GlideScope Video Laryngoscope Titanium Single-Use (SU) Blades, Verathon Incorporated / VERATHON MEDICAL (EUROPE) B.V. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | GlideScope Video Laryngoscope Titanium Single-Use (SU) Blades, Verathon Incorporated / VERATHON MEDICAL (EUROPE) B.V. |
| Manufacturer | Lot recall for GlideScope Video Laryngoscope Titanium Single-Use (SU) Blades, Verathon Incorporated / VERATHON MEDICAL (EUROPE) B.V. |
| Models | 0574-0131, 0574-0130, 0270‐0772, 98011, 0270-0769, 093015, 0270-0771, 0574‐0130, 010101, 0270‐0769, 082115, 0574-0132 and 23 more |
| Date | Mar 22, 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