International safety notice
Recall of the Smith & Nephew products Remove and Skin-Prep wipes that are co-packaged in various batches of the Blom-Singer Adjustable Tracheostoma Valve Kit, InHealth Technologies
Germany / BfArM · DEU · Jul 8, 2011
Key facts
| Title | Recall of the Smith & Nephew products Remove and Skin-Prep wipes that are co-packaged in various batches of the Blom-Singer Adjustable Tracheostoma Valve Kit, InHealth Technologies |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Smith & Nephew products Remove and Skin-Prep wipes that are co-packaged in various batches of the Blom-Singer Adjustable Tracheostoma Valve Kit, InHealth Technologies |
| Manufacturer | Recall of the Smith & Nephew products Remove and Skin-Prep wipes that are co-packaged in various batches of the Blom-Singer Adjustable Tracheostoma Valve Kit, InHealth Technologies |
| Models | 965053, 979331, 01-805-684-9337, 93013, 960796, 955895, 964214, 971679, 3006760724-04, 01-805-684-8594, 982496, 981833 and 16 more |
| Date | Jul 8, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 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