Organ Recovery Systems recalls
Organ Recovery Systems has 2 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 11 Mar 2020. The most frequent reason is lead & heavy metals.
Total recalls2since 2017
Last 12 months0reported
Class I00% of total
Ongoing0latest 11 Mar 2020
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 organ recovery systems is recalled
Product types
By year
All organ recovery systems recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | LKT200 Perfusion Circuit, part of Lifeport Kidney Perfusion recalled | Organ Recovery Systems | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | SPS-1, Static Preservation Solution [1 or bags], Sterile recalled | Organ Recovery Systems | Sterility | 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.