International safety notice
Lot recall of sterile packaging of Guide Wire(s), K-Wire(s) and Intramedullary Pin Metaizeau, Stryker Trauma GmbH
Germany / BfArM · DEU · Feb 11, 2016
Key facts
| Title | Lot recall of sterile packaging of Guide Wire(s), K-Wire(s) and Intramedullary Pin Metaizeau, Stryker Trauma GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of sterile packaging of Guide Wire(s), K-Wire(s) and Intramedullary Pin Metaizeau, Stryker Trauma GmbH |
| Manufacturer | Lot recall of sterile packaging of Guide Wire(s), K-Wire(s) and Intramedullary Pin Metaizeau, Stryker Trauma GmbH |
| Models | K287909, K895099, K0B6D60, K209217, K198568, K862934, K0DBC81, K533002, K0D18F9, K608325, 18060093S, K390254 and 3604 more |
| Date | Feb 11, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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