ABH Nature's Products Recalls All Dietary Supplements for cGMP Violations
ABH Nature's Products Inc. is recalling all dietary supplements under a consent decree because they were prepared, packed, or held in violation of current good manufacturing practice regulations.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class II. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), particularly when associated with significant regulatory violations like cGMP breaches.
Plain-English summary
ABH Nature's Products Inc. is recalling all dietary supplements manufactured and distributed by the company. The recall was ordered by the U.S. Food and Drug Administration through a consent decree.
The agency determined that the products were prepared, packed, or held in violation of current good manufacturing practice (cGMP) regulations. The source text does not specify particular contaminants, specific product names, or lot numbers.
The recall is classified as FDA Class II. Consumers who have purchased these products should stop using them and contact the recalling firm for further instructions.
The recalled product
- Product
- All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
- Manufacturer
- ABH Nature's Products, Inc.
- Category
- Food — Dietary Supplements
- Hazard
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)
- To be determined
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · ABH Nature's Products, Inc.
See all →- CriticalABH Nature's Products Recalls Arthri-D 120ct Due to Salmonella Risk
FDA (Food) · 2018-02-21
- SevereABH Nature's Products Recalls Zero for Him Due to Salmonella Risk
FDA (Food) · 2018-02-21
Same hazard · cGMP violation
See all →- HighHand Sanitizer Recalled Due to Manufacturing Practice Deviations
FDA (Drugs) · 2023-02-08
- ModeratePyrogenium Homeopathic Remedy Recalled for Manufacturing Process Violations
FDA (Drugs) · 2022-06-22
- ModerateDrug Recall: PEPTIME Energy Caffeine Tablets cGMP Violations
FDA (Drugs) · 2022-02-09
- ModerateDrug Recall: PAINAID Tablets for Manufacturing Deviations
FDA (Drugs) · 2022-02-09
- ModerateCalvin Scott Recalls Diethylpropion Tablets Due to Stability Deviations
FDA (Drugs) · 2020-10-14