International safety notice
Stop of use for the products i-Visc ® 1.0, 1.4, 1.6 Sodium Hyaluronate and i-Visc ® 2.0 Hydroxypropyl Methylcellulose, i-Medical Ophthalmic International Heidelberg GmbH
Germany / BfArM · DEU · Jun 27, 2014
Key facts
| Title | Stop of use for the products i-Visc ® 1.0, 1.4, 1.6 Sodium Hyaluronate and i-Visc ® 2.0 Hydroxypropyl Methylcellulose, i-Medical Ophthalmic International Heidelberg GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the products i-Visc ® 1.0, 1.4, 1.6 Sodium Hyaluronate and i-Visc ® 2.0 Hydroxypropyl Methylcellulose, i-Medical Ophthalmic International Heidelberg GmbH |
| Manufacturer | Stop of use for the products i-Visc ® 1.0, 1.4, 1.6 Sodium Hyaluronate and i-Visc ® 2.0 Hydroxypropyl Methylcellulose, i-Medical Ophthalmic International Heidelberg GmbH |
| Models | 13G75, 13M37, 12G46, 13B21, 13L23, 12E25, 13H87, 90-20, 13D41, 68229, 12L82, 13K06 and 17 more |
| Date | Jun 27, 2014 |
| 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