FDA Food recall · Reported August 9, 2017
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.
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Professional Complementary Health Formulas, LLC recalled Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvabl… - a moderate-severity action.
Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvabl… was recalled by Professional Complementary Health Formulas, LLC in August 9, 2017. Reason: Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not dec…. Check the official notice for the remedy. Verify recall #F-3348-2017 with the FDA Food before acting.
The recall
Professional Complementary Health Formulas, LLC issued this moderate-severity FDA Food recall-Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not dec….
- Moderate
- severity level
- Class II
- classification
- August 9, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-3348-2017 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 - 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,472 drugs & medications 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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-3348-2017 |
| Date reported | August 9, 2017 |
| Date initiated | July 21, 2017 |
| Recalling firm | Professional Complementary Health Formulas, LLC |
| Firm location | Lake Oswego, OR |
| Affected scope | 2178/60 tablets Bottles |
| Distribution | distributed in 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, and WI and in the following countries: Canada and United Kingdom |
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-3348-2017) 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.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. 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 (Moderate), closest by report date among other firms and states.
Similar Drugs & Medications · 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