International safety notice
Batch recall of TC-PLUS Primary Fixed Tibial Components VKS (cemented and non-cemented), Smith & Nephew Orthopaedics AG
Germany / BfArM · DEU · Mar 16, 2016
Key facts
| Title | Batch recall of TC-PLUS Primary Fixed Tibial Components VKS (cemented and non-cemented), Smith & Nephew Orthopaedics AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Batch recall of TC-PLUS Primary Fixed Tibial Components VKS (cemented and non-cemented), Smith & Nephew Orthopaedics AG |
| Manufacturer | Batch recall of TC-PLUS Primary Fixed Tibial Components VKS (cemented and non-cemented), Smith & Nephew Orthopaedics AG |
| Models | R-2016-11, B1513062, C1507850, B1511100, B1503362, 75000283, B1501722, C1507852, B1509884, B1512659, 75000280, B1509344 and 44 more |
| Date | Mar 16, 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