Ansar Group recalls
Ansar Group has 1 recall on record with the FDA and USDA, the earliest in 2014 and the latest reported on 27 Aug 2014. The most frequent reason is device malfunction.
Total recalls1since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 27 Aug 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why ansar group is recalled
Product types
By year
All ansar group recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Blood pressure (BP) circuit of the Ansar Anx-3.0 Autonomic recalled | Ansar Group | Device Malfunction | Nationwide |
About 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.