FDA Food recall F-0216-2014
Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle
- FDA Food
- Class I
- terminated
- Published 2013-11-27
On 2013-11-27 the FDA classified a Class I recall of Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle by New Algae, citing flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0216-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-10-23 |
| Published | 2013-11-27 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | New Algae |
| Distribution | US |
Product
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 microalgae (aph. flos-aquae) and chicken cartilage. The serving size is 3 capsules and the suggested use is one 3 capsule serving per day.
Reason
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Identifiers
| code_info | Lot EY1, manufacturing date of 8/2013. (product expires by August 2015) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0216-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.