International safety notice
Neaktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Feb 2, 2018
Key facts
| Title | Neaktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | REFOBACIN PLUS/ OPTIPAC 80 REFOBACIN/ OPTIPAC 40 REFOBACIN/ OPTIPAC 60 REFOBACIN/ OPTIPAC KNEE REFOBACIN PLUS, REFOBACIN BONE CEMENT |
| Manufacturer | BIOMET Orthopaedics Switzerland GmbH |
| Models | 4003920001, 718ABA3103, 0001243555, 718ABD2003, 714CAB1601, 714CAD0505, A719A07288, A722B08910, B720BD2002, 718AAD0505, A710D05600, B712A06130 and 88 more |
| Event type | Safety Notice |
| Date | Feb 2, 2018 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes 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