Stelkast recalls
Stelkast has 3 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 21 Jan 2015. The most frequent reason is lead & heavy metals.
Total recalls3since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 21 Jan 2015
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why stelkast is recalled
Product types
By year
All stelkast recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Recalled product recalled by Stelkast | Stelkast | Lead & Heavy Metals | 10 states |
| Device | CLASS II | SC2316, Distal Femoral Augment recalled by Stelkast | Stelkast | Sterility | Nationwide |
| Device | CLASS II | Cross-over Acetabular Shell and Liner Hip System recalled by Stelkast | Stelkast | 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.