International safety notice
Lot Recall of the totally implantable venous access system PORT PUR Katheter 6Fr (intravenous), Create Medic Co., Ltd.
Germany / BfArM · DEU · Mar 19, 2010
Key facts
| Title | Lot Recall of the totally implantable venous access system PORT PUR Katheter 6Fr (intravenous), Create Medic Co., Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot Recall of the totally implantable venous access system PORT PUR Katheter 6Fr (intravenous), Create Medic Co., Ltd. |
| Manufacturer | Lot Recall of the totally implantable venous access system PORT PUR Katheter 6Fr (intravenous), Create Medic Co., Ltd. |
| Models | H9120004, TH9120001, TH91200041, 45770, H9120001 |
| Date | Mar 19, 2010 |
| 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