CAP-BIOTIN 100 MG — Class I drug recall D-1068-2016
Terminated recall by Reliable Rexall-A Compounding Pharmacy, reported 2016-07-13, distributed in CA, HI, NM. Labeling: Label Mix-Up: Products labeled Biotin 100 mg found to contain 4-aminopyridine
| Recall number | D-1068-2016 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Reliable Rexall-A Compounding Pharmacy, San Francisco, CA, United States |
| Recall initiated | 2016-03-25 |
| Classified | 2016-07-06 |
| Reported by FDA | 2016-07-13 |
| Terminated | 2017-04-10 |
| Distributed | CA, HI, NM |
| Reason classes | labeling |
Product
CAP-BIOTIN 100 MG, Rx Only, Compounded by RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.
Reason for recall
Labeling: Label Mix-Up: Products labeled Biotin 100 mg found to contain 4-aminopyridine
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-1068-2016. 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.