Del Mar Reynolds Medical recalls
Del Mar Reynolds Medical has 8 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 24 May 2017. The most frequent reason is device malfunction.
Total recalls8since 2012
Last 12 months0reported
Class I338% of total
Ongoing0latest 24 May 2017
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 3 38%Class II 5 63%Class III 0 0%
Why del mar reynolds medical is recalled
Product types
By year
All del mar reynolds medical recalls, newest first
8 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Spacelabs Healthcare Arkon Anesthesia Delivery System recalled | Del Mar Reynolds Medical | Packaging Defects | 6 states |
| Device | CLASS II | Arkon Anesthesia Delivery System recalled by Del Mar Reynolds Medical | Del Mar Reynolds Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Spacelabs Pediatric Flow Sensor Kit, PN recalled | Del Mar Reynolds Medical | Labeling Errors | LA, NC, WA |
| Device | CLASS I | SpaceLabs Arkon Anesthesia Delivery System recalled | Del Mar Reynolds Medical | Device Malfunction | Nationwide |
| Device | CLASS I | CAS I/II Absorbers that are parts of the BleaseSirius recalled | Del Mar Reynolds Medical | Other | Nationwide |
| Device | CLASS II | Spacelabs Arkon Anesthesia Workstation recalled | Del Mar Reynolds Medical | Device Malfunction | SC |
| Device | CLASS I | Spacelabs BleaseSirius Anesthesia Workstation recalled | Del Mar Reynolds Medical | Device Malfunction | Nationwide |
| Device | CLASS II | BleaseFocus Anesthesia Workstation recalled by Del Mar Reynolds Medical | Del Mar Reynolds Medical | 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.