GM Manufacturing Recalls Detoxification Plus Dietary Supplements
GM Manufacturing is recalling Detoxification Plus dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 cGMP violations without reported illnesses or specific high-risk pathogens, fitting the criteria for moderate severity.
Plain-English summary
GM Manufacturing Inc. is recalling 338 bottles of Detoxification Plus dietary supplements. The product was distributed in California and carries the code 724EXP08.2015.
The recall was initiated because the dietary supplements were found to have significant violations of the current good manufacturing practice (cGMP) regulations. The FDA has classified this recall as Class II.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Detoxification Plus, Bottles
- Manufacturer
- GM Manufacturing Inc.
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 338
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)
- 724EXP08.2015
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 46 recalled by GM Manufacturing Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 46 products in this recall →Related recalls
Same manufacturer · GM Manufacturing Inc.
See all →- ModerateGM Manufacturing Recalls Samurai-X Blister Packs for cGMP Violations
FDA (Food) · 2014-08-06
- ModerateGM Manufacturing Recalls Green Coffee Bean Supplements for cGMP Violations
FDA (Food) · 2014-08-06
- ModerateGM Manufacturing Recalls Garcinia Cambogia Extract Capsules for cGMP Violations
FDA (Food) · 2014-08-06
- ModerateGM Manufacturing Recalls Una De Gato Dietary Supplements for cGMP Violations
FDA (Food) · 2014-08-06
- ModerateGM Manufacturing Recalls Via-Max Gold Supplements for cGMP Violations
FDA (Food) · 2014-08-06
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: PAINAID Tablets for Manufacturing Deviations
FDA (Drugs) · 2022-02-09
- ModerateDrug Recall: PEPTIME Energy Caffeine Tablets cGMP Violations
FDA (Drugs) · 2022-02-09
- ModerateCalvin Scott Recalls Diethylpropion Tablets Due to Stability Deviations
FDA (Drugs) · 2020-10-14
Similar recalls
- ModerateBasic Reset Recalls Beta Factor Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Trim Up Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Body Mass Reset for CGMP Non-Compliance
FDA (Food) · 2019-11-27
- ModerateDuy Drugs Recalls Cardiovid Plus Dietary Supplement for CGMP Violations
FDA (Food) · 2017-08-16
- ModerateBasic Reset Recalls GH-C Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateHealth One Pharmaceuticals Recalls GLU Dietary Supplements for cGMP Violations
FDA (Food) · 2015-04-08