F-3348-2017 Class II Terminated
FDA food recall F-3348-2017 was initiated by Professional Complementary Health Formulas, LLC on Jul 21, 2017 and is designated Class II. Reason for recall: Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk. The recall status is terminated (terminated Mar 21, 2018). Affected quantity: 2178/60 tablets Bottles.
Recall Details
- Product Type
- Food
- Report Date
- Aug 9, 2017
- Initiation Date
- Jul 21, 2017
- Termination Date
- Mar 21, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2178/60 tablets Bottles
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.
Distribution Pattern
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
Code Information
Lot numbers: 409017; 503019; 508060; 603032; and 701039. QR Codes: 1409002; 1505019; 1603007; 1607022; and 1701013. QR codes are interpreted as below: " The first two digits represent the year in which the product was ordered or manufactured; " The second two digits represent the month in which the product was ordered or manufactured; and " The last three digits represent the products place in a sequential list of products ordered during that month and year.
Source
- Dataset
- openFDA food recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for F-3348-2017
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 8, 2026