New Algae Company
FEI 3022187 · United States
Per FDA, as of 2026-10-31 · Sources: FDA Data Dashboard, Import Alerts, Enforcement Reports
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Import alerts
0
Import refusals (5 years)
0
Warning letters
0
Last FDA action
2013-10-23
13 years ago
FDA record
- 2013-10-23RecallRecall F-0215-2014 · Class 1 · EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different packets of capsules - a "Before" packet and an "After" packet. The suggested use for the After packet is one packet (or 6 capsu…Source: FDA Enforcement Reports
- 2013-10-23RecallRecall F-0216-2014 · Class 1 · Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle. The Flex product is a dietary supplement in capsule form containing vegetable glucosamine HCL, chondroitin sulfate (shark cartilage), organic mic…Source: FDA Enforcement Reports