Allergan recalls
Allergan has 26 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 10 Feb 2021. 16 are still ongoing. The most frequent reason is foreign material.
Total recalls26since 2015
Last 12 months0reported
Class I1558% of total
Ongoing16latest 10 Feb 2021
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 15 58%Class II 8 31%Class III 3 12%
Why allergan is recalled
Product types
By year
Ongoing allergan recalls
16 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | XEN Gel Stent recalled by Allergan | Allergan | Sterility | Nationwide |
| Device | CLASS I | Ritz Princess, Biocell, Intrashiel recalled by Allergan | Allergan | Foreign Material | Nationwide |
| Device | CLASS I | McGhan BioDIMENSIONAL silicone-Filled Breast Implants, style recalled | Allergan | Foreign Material | Nationwide |
| Device | CLASS I | Natrelle 510, TruForm, Dual-Gel, Biocell, Styles LX, MX, FX recalled | Allergan | Foreign Material | Nationwide |
| Device | CLASS I | Natrelle 410, Highly Cohesive Anatomically Shaped recalled by Allergan | Allergan | Foreign Material | Nationwide |
| Device | CLASS I | Natrelle 133 Tissue Expanders recalled by Allergan | Allergan | Foreign Material | Nationwide |
All allergan recalls, newest first
26 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.