Professional Formulas Sublinqual B12 High-Potency dietary supplement — Class II food recall F-3348-2017
Terminated recall by Professional Complementary Health Formulas, LLC, reported 2017-08-09, distributed in AZ, CA, CO, CT, FL, GA, HI, ID…. Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not decl
| Recall number | F-3348-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Professional Complementary Health Formulas, LLC, Lake Oswego, OR, United States |
| Recall initiated | 2017-07-21 |
| Classified | 2017-08-03 |
| Reported by FDA | 2017-08-09 |
| Terminated | 2018-03-21 |
| Distributed | AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MT, NC, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, WA, WI |
| Countries outside the US | CA, GB |
| Reason classes | labeling |
| Lot numbers | 1409002, 1505019, 1603007, 1607022, 1701013, 409017, 503019, 508060, 603032, 701039 |
Product
Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic bottles. Adhesive label with White, black red and green print; bottle has a heat-shrink band. UPC code 8 40851 10054 0.
Reason for recall
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
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/F-3348-2017. 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.