International safety notice
Corrective action and recall for DELFIA and AutoDELFIA Neonatal-17α-OH-Progesteron-Kits, PerkinElmer
Germany / BfArM · DEU · Dec 14, 2009
Key facts
| Title | Corrective action and recall for DELFIA and AutoDELFIA Neonatal-17α-OH-Progesteron-Kits, PerkinElmer |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | DELFIA and AutoDELFIA Neonatal-17α-OH-Progesteron-Kits, PerkinElmer |
| Manufacturer | Corrective action and recall for DELFIA and AutoDELFIA Neonatal-17α-OH-Progesteron-Kits, PerkinElmer |
| Models | R2009017, 560684, 559939, B024-112, 8024-112, 558875, 559754, B024-1, NEONATAL-17A-OH, NEONATAL-17A.OHRO, 561098, NEONATAL.17A-OH and 15 more |
| Date | Dec 14, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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