International safety notice
Recall of Shoulder Suspension Tower, Arthrex / Allen Medical Systems / Hill-Rom SAS
Germany / BfArM · DEU · Jan 27, 2017
Key facts
| Title | Recall of Shoulder Suspension Tower, Arthrex / Allen Medical Systems / Hill-Rom SAS |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Shoulder Suspension Tower, Arthrex / Allen Medical Systems / Hill-Rom SAS |
| Manufacturer | Recall of Shoulder Suspension Tower, Arthrex / Allen Medical Systems / Hill-Rom SAS |
| Models | 56330, 501822, 14550, 510751, MOD1257, D-790336-A, D-790336-A1, 510738, 501895, 01720, 2016-11, 19782664280 and 7 more |
| Date | Jan 27, 2017 |
| 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