International safety notice
Recall for CELL-DYN Sapphire Hemoglobin Reagent Syringe, Abbott
Germany / BfArM · DEU · Jan 19, 2009
Key facts
| Title | Recall for CELL-DYN Sapphire Hemoglobin Reagent Syringe, Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | CELL-DYN Sapphire Hemoglobin Reagent Syringe, Abbott |
| Manufacturer | Recall for CELL-DYN Sapphire Hemoglobin Reagent Syringe, Abbott |
| Models | SYR-S12E-0243, SYR-S12E-0248, FA10DEC2008, SYR-S12E-0232, SYR-S12E-0213, SYR-S12E-0066, SYR-S12E-0236, SYR-S12E-0239, SYR-S12E-0130, SYR-S12E-0074, SYR-S12E-0097, SYR-S12E and 26 more |
| Date | Jan 19, 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