CLASS II Food recall · Reported 9 Aug 2017 · FDA Enforcement Report

Professional Formulas Sublinqual B12 High-Potency dietary recalled

Professional Complementary Health Formulas is recalling Professional Formulas Sublinqual B12 High-Potency dietary supplement dissolvable tablet, distributed in 34 states. The recall was initiated on 21 Jul 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 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.
Quantity recalled2178/60 tablets Bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-3348-2017
FDA event ID
77806
Recalling firm
Professional Complementary Health Formulas, Lake Oswego, OR
Classification
Class II
Status
Terminated
Recall initiated
21 Jul 2017
FDA classified
3 Aug 2017
Reported
9 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Milk
Product category
Vitamins

Timeline

21 Jul 2017Recall initiated by company
3 Aug 2017Classified by FDA+13 days
9 Aug 2017Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.

Product as listed by the FDA

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.

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

ArizonaCaliforniaColoradoConnecticutFloridaGeorgiaHawaiiIdahoIllinoisIndianaKansasLouisianaMassachusettsMarylandMaineMichiganMontanaNorth CarolinaNew JerseyNew Mexico

Questions about this recall

Is Professional Formulas Sublinqual B12 High-Potency dietary supplement dissolvable tablet recalled?

Yes. Professional Complementary Health Formulas recalled Professional Formulas Sublinqual B12 High-Potency dietary supplement dissolvable tablet on 21 Jul 2017. The recall is Class II and its status is Terminated. Recall number F-3348-2017.

Why was it recalled?

Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.

Which lots are affected?

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.

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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