International safety notice
Lot recall of IBS-PEEK TLIF II, Peter Brehm GmbH
Germany / BfArM · DEU · Jul 25, 2016
Key facts
| Title | Lot recall of IBS-PEEK TLIF II, Peter Brehm GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of IBS-PEEK TLIF II, Peter Brehm GmbH |
| Manufacturer | Lot recall of IBS-PEEK TLIF II, Peter Brehm GmbH |
| Models | FB-5.06.01-06, 91085, R-20160706-8, FB-5.06.01-07, 22959-14-05, 22958-08-05, 22957-08-05, 22957-12-05, 22958-12-05, 22957-06-05, 22957-14-05, D-91085 and 8 more |
| Date | Jul 25, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 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