CHIROTHIN Dietary Supplement — Class III drug recall D-1569-2014
Terminated recall by ChiroNutraceutical LLC, reported 2014-09-17, distributed nationwide. Marketed without an Approved NDA/ANDA; Product contains unapproved hHCG.
| Recall number | D-1569-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ChiroNutraceutical LLC, Chesterfield, MO, United States |
| Recall initiated | 2014-08-20 |
| Classified | 2014-09-09 |
| Reported by FDA | 2014-09-17 |
| Terminated | 2015-06-16 |
| Distributed | Nationwide (US) |
| Quantity | 12,948 bottles |
| Reason classes | unapproved product |
| Lot numbers | 072010-22, 072010-23, 072010-25, 072010-26, 072010-27, 072010-29, 072010-30, 072010-31, 072010-33, 072010-34, 072010-36, 072010-39, 072010-43, 072010-48 |
| Expiration dates | 2013-12, 2014-01, 2014-03, 2014-04, 2014-05, 2014-07, 2014-08, 2014-09, 2014-11, 2015-01, 2015-02, 2015-05, 2015-06, 2015-10 |
Product
CHIROTHIN Dietary Supplement, 2 Fl Oz (60 ml), OTC. Manufactured for ChiroNeutraceutical, 877-377-7636, Chesterfield, MO 63005.
Reason for recall
Marketed without an Approved NDA/ANDA; Product contains unapproved hHCG.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1569-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.