Philips Medical Systems North America Co. Phillips recalls
Philips Medical Systems North America Co. Phillips has 2 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 16 Jan 2013.
Total recalls2since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 16 Jan 2013
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 philips medical systems north america co. phillips is recalled
Product types
By year
All philips medical systems north america co. phillips recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Philips and Laerdal brands of HeartStart HS1 Defibrillator Family recalled | Philips Medical Systems North America Co. Phillips | Other | Nationwide |
| Device | CLASS II | Philips HeartStart FRx 861304 Automated External Defibrillator recalled | Philips Medical Systems North America Co. Phillips | Other | 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.