B12 Supplement (Professional Formulas) – Undeclared Milk (2017)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Professional Complementary Health Formulas, LLC
Lot Codes / Batch Numbers
Lot numbers: 409017, 503019, 508060, 603032, and 701039. QR Codes: 1409002, 1505019, 1603007, 1607022, " The second two digits represent the month in which the product was ordered or manufactured
Products Sold
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.
Professional Complementary Health Formulas, LLC is recalling Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in due to Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, LA, ME, MD, MA, MI, MT, NV, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, WA, WI
Page updated: Jan 6, 2026