Professional Formulas Sublinqual B12 High-Potency dietary supplement
Recalling firm: Professional Complementary Health Formulas, LLC
Why it was recalled
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
The exact 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.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA 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.
Recall details
- Recall number
- F-3348-2017
- Event ID
- 77806
- FDA status
- Terminated
- Initiated
- Jul 21, 2017
- Reported
- Aug 9, 2017
- Classified
- Aug 3, 2017
- Terminated
- Mar 21, 2018
- Quantity
- 2178/60 tablets Bottles
- Location
- Lake Oswego, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
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
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.