FDA recall F-3348-2017

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.

Reason for recall

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

Distribution

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

Key facts

Status

Terminated

Initiation date

2017-07-21

Report date

2017-08-09

Termination date

2018-03-21

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lake Oswego, OR, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-3348-2017