FDA Food recall · Reported November 27, 2013
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.
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
New Algae Company recalled Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottl… - a critical-severity action.
Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottl… was recalled by New Algae Company in November 27, 2013. Reason: Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.. Check the official notice for the remedy. Verify recall #F-0216-2014 with the FDA Food before acting.
The recall
New Algae Company issued this critical-severity FDA Food recall-Flex dietary supplement product is recalled because the finished label does not declare shark cartilage..
- Critical
- severity level
- Class I
- classification
- November 27, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0216-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,457 food recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
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 for recall
Flex dietary supplement product is recalled because the finished label does not declare shark cartilage.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-0216-2014 |
| Date reported | November 27, 2013 |
| Date initiated | October 23, 2013 |
| Recalling firm | New Algae Company |
| Firm location | Klamath Falls, OR |
| Affected scope | 103 bottles (90 capsules per bottle) |
| Distribution | Distributed nationwide. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0216-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Nationwide recalls with similar severity or category timing
Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Critical), closest by report date among other firms and states.
Similar Food · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026