International safety notice
Batch / lot recall of LMA MAD Nasal Intranasal Mucosal Atomization Device, Teleflex Medical
Germany / BfArM · DEU · Nov 2, 2016
Key facts
| Title | Batch / lot recall of LMA MAD Nasal Intranasal Mucosal Atomization Device, Teleflex Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Batch / lot recall of LMA MAD Nasal Intranasal Mucosal Atomization Device, Teleflex Medical |
| Manufacturer | Batch / lot recall of LMA MAD Nasal Intranasal Mucosal Atomization Device, Teleflex Medical |
| Models | 160200, 160814, 160327, MAD140OS, MAD300, 160225, 160631, MAD100OS, 160218, 160500, MAD300B, 160440 and 65 more |
| Date | Nov 2, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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