Konica Minolta Medical Imaging USA recalls
Konica Minolta Medical Imaging USA has 6 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 4 Jul 2018. The most frequent reason is device malfunction.
Total recalls6since 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 4 Jul 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 6 100%Class III 0 0%
Why konica minolta medical imaging usa is recalled
Product types
By year
All konica minolta medical imaging usa recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | ImagePilot, Model No. D9MA recalled by Konica Minolta Medical | Konica Minolta Medical Imaging USA | Device Malfunction | Nationwide |
| Device | CLASS II | CS-7, Model No. A4C1 recalled by Konica Minolta Medical | Konica Minolta Medical Imaging USA | Device Malfunction | Nationwide |
| Device | CLASS II | Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP recalled | Konica Minolta Medical Imaging USA | Device Malfunction | 35 states |
| Device | CLASS II | Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8WA recalled | Konica Minolta Medical Imaging USA | Device Malfunction | 35 states |
| Device | CLASS II | Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A9RP recalled | Konica Minolta Medical Imaging USA | Device Malfunction | 35 states |
| Device | CLASS II | Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8AR recalled | Konica Minolta Medical Imaging USA | Device Malfunction | 35 states |
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.