International safety notice
Batch recall for ENT single-use suction tubes, Spiggle & Theis Medizintechnik GmbH
Germany / BfArM · DEU · Feb 18, 2016
Key facts
| Title | Batch recall for ENT single-use suction tubes, Spiggle & Theis Medizintechnik GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ENT single-use suction tubes, Spiggle & Theis Medizintechnik GmbH |
| Manufacturer | Batch recall for ENT single-use suction tubes, Spiggle & Theis Medizintechnik GmbH |
| Models | 811635072, COKSDE33, 52076, 014443, 3010040, GENODED1PAF, 3110030, 3010030, 014808, 014557, 51491, D-51491 and 4 more |
| Date | Feb 18, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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