International safety notice
Recall for Terumo® AL6X Arterial Blood Line Filter - Terumo Tubing Sets, Terumo
Germany / BfArM · DEU · Nov 20, 2013
Key facts
| Title | Recall for Terumo® AL6X Arterial Blood Line Filter - Terumo Tubing Sets, Terumo |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Terumo® AL6X Arterial Blood Line Filter - Terumo Tubing Sets, Terumo |
| Manufacturer | Recall for Terumo® AL6X Arterial Blood Line Filter - Terumo Tubing Sets, Terumo |
| Models | CX-IT226X, TP7104, CX-IT241X, CX-ROC25AL6X, 1212047, 1211169, 1208014, 1201127, CX-DB325X, 1210136, CX-ROCRXAL6X, 1303235 and 105 more |
| Date | Nov 20, 2013 |
| 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