International safety notice
Lot recall of BT2000 (SKU 014613) and CPT2000 (SKU 014623) Manifold Kits, ACIST Medical Systems Inc. / ACIST Europe BV
Germany / BfArM · DEU · Feb 5, 2016
Key facts
| Title | Lot recall of BT2000 (SKU 014613) and CPT2000 (SKU 014623) Manifold Kits, ACIST Medical Systems Inc. / ACIST Europe BV |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of BT2000 (SKU 014613) and CPT2000 (SKU 014623) Manifold Kits, ACIST Medical Systems Inc. / ACIST Europe BV |
| Manufacturer | Lot recall of BT2000 (SKU 014613) and CPT2000 (SKU 014623) Manifold Kits, ACIST Medical Systems Inc. / ACIST Europe BV |
| Models | NL808081196B01, 30159397, BT2000, 13485, CPT2000, 014623, 014613 |
| Date | Feb 5, 2016 |
| 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