International safety notice
Recall for Vitrax II, Ophthalmic Viscosurgical Devices (Sodium Hyaluronate 3%)", 0,65 ml, Abbott
Germany / BfArM · DEU · Nov 3, 2009
Key facts
| Title | Recall for Vitrax II, Ophthalmic Viscosurgical Devices (Sodium Hyaluronate 3%)", 0,65 ml, Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Vitrax II, Ophthalmic Viscosurgical Devices (Sodium Hyaluronate 3%)", 0,65 ml, Abbott |
| Manufacturer | Recall for Vitrax II, Ophthalmic Viscosurgical Devices (Sodium Hyaluronate 3%)", 0,65 ml, Abbott |
| Models | 018476, 013526, 014409, 018477, 023430, VT465, 014410, 016376, 373-390, 76275, 012936, GESCHÄFGF0HRER and 23 more |
| Date | Nov 3, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 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