International safety notice
Batch recall of NewBreez intralaryngeal prosthesis, PROTiP Medical
Germany / BfArM · DEU · Dec 15, 2016
Key facts
| Title | Batch recall of NewBreez intralaryngeal prosthesis, PROTiP Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Batch recall of NewBreez intralaryngeal prosthesis, PROTiP Medical |
| Manufacturer | Batch recall of NewBreez intralaryngeal prosthesis, PROTiP Medical |
| Models | LOT-15-00017, P0009, IF16001, P0019, LOT-16-00006, LOT-1500028, LOT-15O004, F-67000, P0018, LOT-15-00015, LOT-IS-00003, LOT-16-00004 and 2 more |
| Date | Dec 15, 2016 |
| 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