Mindray DS USA, Inc. d.b.a. Mindray North America recalls
Mindray DS USA, Inc. d.b.a. Mindray North America has 9 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 3 Apr 2013. The most frequent reason is device malfunction.
Total recalls 9 since 2012
Last 12 months 0 reported
Class I 2 22% of total
Ongoing 0 latest 3 Apr 2013
Recalls per month, last 24 months click a bar for that month Severity split
2 22%7 78%0 0%
Why mindray ds usa, inc. d.b.a. mindray north america is recalled
All mindray ds usa, inc. d.b.a. mindray north america recalls, newest first 9 total Reported Class Recall Company Reason Where 3 Apr 2013 Device CLASS II BS-200 Chemistry Analyzer Designed for clinical laboratory use recalled Mindray DS USA, Inc. d.b.a. Mindray North America Labeling Errors NC, TX 20 Feb 2013 Device CLASS II Mindray DS USA, Inc., DPM Central Monitoring System recalled Mindray DS USA, Inc. d.b.a. Mindray North America Device Malfunction Nationwide 6 Feb 2013 Device CLASS II Mindray DPM5 Monitor, a vital signs monitor used on human recalled Mindray DS USA, Inc. d.b.a. Mindray North America Device Malfunction Nationwide 9 Jan 2013 Device CLASS II DPM Central Station Mindray DS USA recalled Mindray DS USA, Inc. d.b.a. Mindray North America Device Malfunction Nationwide 26 Dec 2012 Device CLASS II Mindray V12 Size: N.W.: G.W.: Qty:1 recalled Mindray DS USA, Inc. d.b.a. Mindray North America Temperature Abuse Nationwide 19 Dec 2012 Device CLASS II DPM 6/7 Patient Monitor recalled by Mindray DS USA, Inc. d.b.a. Mindray DS USA, Inc. d.b.a. Mindray North America Temperature Abuse Nationwide 28 Nov 2012 Device CLASS I Mindray A3 Anesthesia Delivery System recalled Mindray DS USA, Inc. d.b.a. Mindray North America Packaging Defects Nationwide 28 Nov 2012 Device CLASS I Mindray A5 Anesthesia Delivery System recalled Mindray DS USA, Inc. d.b.a. Mindray North America Packaging Defects Nationwide 5 Sep 2012 Device CLASS II V Series Patient Monitors recalled by Mindray DS USA, Inc. d.b.a. Mindray DS USA, Inc. d.b.a. Mindray North America 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.