Mortara Instrument recalls
Mortara Instrument has 2 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 24 Jun 2015. The most frequent reason is lead & heavy metals.
Total recalls2since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 24 Jun 2015
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why mortara instrument is recalled
Product types
By year
All mortara instrument recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | ELI 380 Electrocardiograph recalled by Mortara Instrument | Mortara Instrument | Lead & Heavy Metals | 11 states |
| Device | CLASS II | Mortara Surveyor S12 and Surveyor S19 Patient Monitors recalled | Mortara Instrument | Lead & Heavy Metals | 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.