Home › Recall events › New Algae Company recall — Flex, Maximum Flexibility, Item…
New Algae Company recall — Flex, Maximum Flexibility, Item number 21-601, dietary supplement,…
FDA (enforcement) · November 27, 2013 · Class I
- New Algae Company recalled Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per… — an FDA enforcement event posted , classified Class I, covering 2 product entries.
- FDA-stated reason: Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class I
- Status
- Terminated
- Recalling firm
- New Algae Company
- Source ID
- 66630
FDA Enforcement Report search →
Product entries (2)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| F-0215-2014 | 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… | Lot BO1 and AO1, Expiration date Aug 2015 | Distributed nationwide. |
| F-0216-2014 | Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle. The Flex product is a dietary supplement in capsule form… | Lot EY1, manufacturing date of 8/2013. (product expires by August 2015) | Distributed nationwide. |
FDA enforcement entries have no per-recall public URL — verify via the FDA Enforcement Report search using the firm name or a recall number above.
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