International safety notice
Recall for GlucoHEXAL II Blutzuckerteststreifen, Gluco HEXAL II Starterset weiß and GlucoHEXAL II Starterset schwarz, Hexal
Germany / BfArM · DEU · Mar 17, 2010
Key facts
| Title | Recall for GlucoHEXAL II Blutzuckerteststreifen, Gluco HEXAL II Starterset weiß and GlucoHEXAL II Starterset schwarz, Hexal |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | GlucoHEXAL II Blutzuckerteststreifen, Gluco HEXAL II Starterset weiß and GlucoHEXAL II Starterset schwarz, Hexal |
| Manufacturer | Recall for GlucoHEXAL II Blutzuckerteststreifen, Gluco HEXAL II Starterset weiß and GlucoHEXAL II Starterset schwarz, Hexal |
| Models | 5127840, 39179, 5127892, 5127863, 21337, 83602, E09F222577, E09G092577, E09F022577, E09F032577, E09E252577, E09F182577 and 3 more |
| Date | Mar 17, 2010 |
| 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