International safety notice
Lot Recall of the 27 G disposable cannula provided with the Amvisc® und Amvisc® Plus viscoelastic devices, Bausch & Lomb
Germany / BfArM · DEU · Jul 18, 2013
Key facts
| Title | Lot Recall of the 27 G disposable cannula provided with the Amvisc® und Amvisc® Plus viscoelastic devices, Bausch & Lomb |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot Recall of the 27 G disposable cannula provided with the Amvisc® und Amvisc® Plus viscoelastic devices, Bausch & Lomb |
| Manufacturer | Lot Recall of the 27 G disposable cannula provided with the Amvisc® und Amvisc® Plus viscoelastic devices, Bausch & Lomb |
| Models | 024522, D120068D, 4-DIGIT, D120068E, 20040A, D120031A, 8-DIQIT, EMEACS-SUPP01T, D120041B, 20069D, 024493, D120055A and 17 more |
| Date | Jul 18, 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