International safety notice
Urgent Safety Notice / Lot Recall for Bivona Neonatal, Pediatric and Flextend Tracheostomy Tubes, Smiths Medical
Germany / BfArM · DEU · Nov 25, 2011
Key facts
| Title | Urgent Safety Notice / Lot Recall for Bivona Neonatal, Pediatric and Flextend Tracheostomy Tubes, Smiths Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Bivona Neonatal, Pediatric and Flextend Tracheostomy Tubes, Smiths Medical |
| Manufacturer | Urgent Safety Notice / Lot Recall for Bivona Neonatal, Pediatric and Flextend Tracheostomy Tubes, Smiths Medical |
| Models | 60PFP50, 65SP030, 46406-2617, 60PFS40, 60PFSS50, 60P050, 67P040, 65P055, 60SN040, 60PFS25, 67SN035, 65N030 and 91 more |
| Date | Nov 25, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models 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