International safety notice
Recall of Singleday Infusor, Baxter
Germany / BfArM · DEU · Dec 17, 2007
Key facts
| Title | Recall of Singleday Infusor, Baxter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Singleday Infusor, Baxter |
| Manufacturer | Recall of Singleday Infusor, Baxter |
| Models | 2C1071KJPI, 07YÖ€G, 07E055, PRODUKTR0CKRUF, 07H006, 701-349, 2MLTL, 85701, 07E037, 07F061, 95716, 31701-524 and 31 more |
| Date | Dec 17, 2007 |
| 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