International safety notice
Recalls of certain ON-Q-Pumps with Select-A-Flow passive infusion pumps, Flow Corporation
Germany / BfArM · DEU · Sep 7, 2011
Key facts
| Title | Recalls of certain ON-Q-Pumps with Select-A-Flow passive infusion pumps, Flow Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recalls of certain ON-Q-Pumps with Select-A-Flow passive infusion pumps, Flow Corporation |
| Manufacturer | Recalls of certain ON-Q-Pumps with Select-A-Flow passive infusion pumps, Flow Corporation |
| Models | P600X1, 5001810, 5001521, 206-2700, 5001809, 132464, CB6004, 206-2600, 982645, 949-206-2663, P600X2-14, 448-8569 and 32 more |
| Date | Sep 7, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 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