International safety notice
Corrective Action/Recall for MIKRO 120 centrifuge, Andreas Hettich GmbH & Co. KG
Germany / BfArM · DEU · Dec 28, 2010
Key facts
| Title | Corrective Action/Recall for MIKRO 120 centrifuge, Andreas Hettich GmbH & Co. KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | MIKRO 120 centrifuge, Andreas Hettich GmbH & Co. KG |
| Manufacturer | Corrective Action/Recall for MIKRO 120 centrifuge, Andreas Hettich GmbH & Co. KG |
| Models | 078503, DE45653700750213, DE49643500700000002929, DEUTDESS653, 643901, 31.12.2011, 20-S04, ATM120-S03, 78532, 7057.00, 09.12.2010, 479004 and 15 more |
| Date | Dec 28, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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