International safety notice
Corrective action for the products Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-11 and Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-13, Stryker Trauma GmbH
Germany / BfArM · DEU · Jul 22, 2014
Key facts
| Title | Corrective action for the products Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-11 and Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-13, Stryker Trauma GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the products Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-11 and Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-13, Stryker Trauma GmbH |
| Manufacturer | Corrective action for the products Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-11 and Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-13, Stryker Trauma GmbH |
| Models | K07F95F, K019A3C, K032811, 24232, K031467, RA2014-101, 2.12-1, 1806-1406S, K032812, K074529, K031468, 2014-101 and 10 more |
| Date | Jul 22, 2014 |
| 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