International safety notice
Urgent field safety notice for AFX Endovascular AAA System / recall of small remaining quantity of original AFX with Strata graft material and AFX2 Main Body (28 mm) and / or Iliac Limbs (20 mm), Endologix International Holdings B.V.
Germany / BfArM · DEU · Jan 18, 2017
Key facts
| Title | Urgent field safety notice for AFX Endovascular AAA System / recall of small remaining quantity of original AFX with Strata graft material and AFX2 Main Body (28 mm) and / or Iliac Limbs (20 mm), Endologix International Holdings B.V. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AFX Endovascular AAA System / recall of small remaining quantity of original AFX with Strata graft material and AFX2 Main Body (28 mm) and / or Iliac Limbs (20 mm), Endologix International Holdings B.V. |
| Manufacturer | Urgent field safety notice for AFX Endovascular AAA System / recall of small remaining quantity of original AFX with Strata graft material and AFX2 Main Body (28 mm) and / or Iliac Limbs (20 mm), Endologix International Holdings B.V. |
| Models | F00820-09, F00820-78, BA25-120, F00412, F00658, BA28-70, BEA28-110, F00726-03, F00820-79, F00443, F00556, I16-55 and 222 more |
| Date | Jan 18, 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