GM Manufacturing Recalls Tiger-X Blister Packs for cGMP Violations
GM Manufacturing is recalling 11,218 units of Tiger-X dietary supplements in California due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
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, which typically involves a situation where use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences. The source cites cGMP violations without reporting specific illnesses or injuries, aligning with a Moderate severity rating.
Plain-English summary
GM Manufacturing Inc. is recalling 11,218 units of Tiger-X, Blister Packs. The product was distributed in California. No specific lot numbers were identified in the recall notice.
The recall was initiated due to significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements. These regulations are designed to ensure that products are consistently produced and controlled according to quality standards.
Consumers who have purchased Tiger-X, Blister Packs should stop using the product and contact GM Manufacturing Inc. for further instructions or a refund.
The recalled product
- Product
- Tiger-X, Blister Packs
- Manufacturer
- GM Manufacturing Inc.
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 11,218
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)
- No lot numbers
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 Detoxification Plus Dietary Supplements
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
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