Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin recall
Recalled by Vertical Pharmaceuticals, Inc. · Bridgewater, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
One (1) lot (21511158) of the OB Complete DHA is being recalled because the label claim for "Omega-3 Fatty Acids" does not match the actual formulation.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical Pharmaceuticals, LLC Sayreville, NJ 08872 UPC 368025049603
Quantity: 5,734 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 number 21511158 with expiry date 10/20/2017
Where it was sold
Alabama Arkansas Arizona California Colorado Florida Georgia Illinois Louisiana Massachusetts Missouri Mississippi North Carolina New Jersey New York Ohio Oklahoma Pennsylvania South Carolina Texas Virginia
FDA's distribution note: AL, AR, AZ, CA, CO, FL, GA, IL, LA, MA, MO, MS, NC, NJ, NY, OH,OK, PA, SC, TX and VA
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
- Vertical Pharmaceuticals, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 10, 2017
- In FDA report of
- May 17, 2017
- Terminated
- Apr 19, 2018
- FDA recall number
- F-2208-2017 · event 77059
- Official record
- FDA enforcement report search