International safety notice
Recall for intrauterine probes (tubes) with lot numbers up to and including lot J13, Varian medical systems
Germany / BfArM · DEU · Sep 19, 2011
Key facts
| Title | Recall for intrauterine probes (tubes) with lot numbers up to and including lot J13, Varian medical systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | intrauterine probes (tubes) with lot numbers up to and including lot J13, Varian medical systems |
| Manufacturer | Recall for intrauterine probes (tubes) with lot numbers up to and including lot J13, Varian medical systems |
| Models | CR-35878, 00531, GM11006150, GM11006200, GM11006180, GM11006130, 1293-542-626, 1-434-979-1540, GM11006140, 1-949-221-7631, 80013, 800360-7909 and 4 more |
| Date | Sep 19, 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