FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Professional Formulas Sublinqual B12 Recall

Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolva…

Professional Complementary Health Formulas, LLC · Lake Oswego, OR

Risk level
Class II
Reported by FDA
Aug 9, 2017
Recall ID
F-3348-2017
Check your lot numberHow we source this data

Summary

Professional Complementary Health Formulas recalled Professional Formulas Sublinqual B12 starting Jul 21, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-3348-2017 on Aug 9, 2017. Reason: Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk. Status: Terminated.

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

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 it was 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 to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-3348-2017
Classification
Class II
Status
Terminated
Recall initiated
Jul 21, 2017
FDA report date
Aug 9, 2017
Quantity
2178/60 tablets Bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Professional Complementary Health Formulas, LLC

Original FDA data

Every field from FDA enforcement report F-3348-2017, exactly as published.

Show all FDA fields
City
Lake Oswego
State
OR
Status
Terminated
Country
United States
Event ID
77806
Address
5550 Rosewood St
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.
Postal code
97035-5371
Report date
Aug 9, 2017
Product type
Food
Recall number
F-3348-2017
Classification
Class II
Recalling firm
Professional Complementary Health Formulas, LLC
Product quantity
2178/60 tablets Bottles
Termination date
Mar 21, 2018
Reason for recall
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Voluntary / mandated
Voluntary: Firm initiated
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.
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
Recall initiation date
Jul 21, 2017
Initial firm notification
Letter
Center classification date
Aug 3, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-3348-2017, published Aug 9, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls