Inositol packaged in white plastic bottle with
Reason Product recalled due to undeclared niacin.
Vitamin B Complex packaged in white plastic bottle labeled in part recall
Recalled by Professional Complementary Health Formulas, LLC · Lake Oswego, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product recalled due to undeclared niacin.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Vitamin B Complex packaged in white plastic bottle labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Vitamin B Complex DIETARY SUPPLEMENT 60 Capsules***Supplement Facts Serving Size: One Capsule***Vitamin B1 (as thiamine Hcl) 80mg 6667% Vitamin B2 (as riboflavin) 80 mg 6154% Vitamin B3 (as niacinamide) 80 mg NE 500% Vitamin B6 (as pyridoxine HCl) 80 mg 4706% Folic acid 667 mcg DFE 167% Vitamin B12 (as cyanocobalamin) 80 mcg 3333% Biotin 300 mcg 1000% Vitamin B5 (as calcium pantothenate) 80 mg 1600% Choline (as bitartrate) 80 mg 15%***Professional Formulas PO Box 2034, Lake Oswego, OR 97035 Recommended Dosage: As a nutritional supplement, take one capsule, or as directed by your healthcare professional***FOR PROFESSIONAL USE ONLY"
Quantity: 299 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 1092715
Where it was sold
Nationwide.
New York Oregon Pennsylvania Utah Wisconsin Wyoming
FDA's distribution note: Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Professional Complementary Health Formulas, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 20, 2021
- In FDA report of
- Feb 8, 2023
- Terminated
- Apr 3, 2023
- FDA recall number
- F-0323-2023 · event 91377
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
Other recalls by Professional Complementary Health Formulas, LLC
Professional Formulas Sublinqual B12 High-Potency dietary supplement
Reason Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.