Vertical Pharmaceuticals Recalls OB Complete Prenatal Multivitamin Due to Labeling Error
Vertical Pharmaceuticals is recalling one lot of OB Complete with DHA Prenatal Multivitamin because the label claim for Omega-3 Fatty Acids does not match the actual formulation.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a labeling discrepancy regarding Omega-3 Fatty Acids. This fits the rubric for moderate severity, as it is a labeling error without reported illnesses or injuries.
Plain-English summary
Vertical Pharmaceuticals, Inc. is recalling one lot (21511158) of OB Complete with DHA Prenatal Multivitamin, 60 softgels. The recall is being conducted because the label claim for "Omega-3 Fatty Acids" does not match the actual formulation of the product.
The affected product is identified by lot number 21511158 and has an expiration date of 10/20/2017. A total of 5,734 bottles were distributed to the states of AL, AR, AZ, CA, CO, FL, GA, IL, LA, MA, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TX, and VA.
Consumers who have this product should check the lot number and expiration date on the packaging. If the product matches the recalled lot, consumers should stop using it and contact their healthcare provider or the manufacturer for further instructions.
The recalled product
- Product
- Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical Pharmaceuticals, LLC Sayreville, NJ 08872 UPC 368025049603
- Manufacturer
- Vertical Pharmaceuticals, Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 5,734
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot number 21511158 with expiry date 10/20/2017
Distribution
Related recalls
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02