International safety notice
Recall / Corrective Action for Uritest 13G Urine reagent Strips, URIT Medical Electronic
Germany / BfArM · DEU · Jan 19, 2010
Key facts
| Title | Recall / Corrective Action for Uritest 13G Urine reagent Strips, URIT Medical Electronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Uritest 13G Urine reagent Strips, URIT Medical Electronic |
| Manufacturer | Recall / Corrective Action for Uritest 13G Urine reagent Strips, URIT Medical Electronic |
| Models | FSCA-20091209, NO.20090227, 2832799, 2288586, 54100, 2804668, 2009-12-09, 280466B, 28A2799, 541001, 100MG, R.C9IINA and 2 more |
| Date | Jan 19, 2010 |
| 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