International safety notice
Baxter recalls the Benja-Mix Verlängerungsset
Germany / BfArM · DEU · Feb 28, 2005
Key facts
| Title | Baxter recalls the Benja-Mix Verlängerungsset |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Baxter recalls the Benja-Mix Verlängerungsset |
| Manufacturer | Baxter recalls the Benja-Mix Verlängerungsset |
| Models | 2.2.2005, «OADR2», 31701-207, 01-207, 018325200, 6179-0, 42976, 01-462, «OADR3», 0-85701, D-85716, 09131 and 2 more |
| Date | Feb 28, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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