Anderson Compounding Pharmacy Recalls HCG Vials Due to Sterility Concerns
Anderson Compounding Pharmacy is recalling HCG 11,000 Units vials nationwide because the product lacks sterility assurance.
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 classified this as an FDA Class II recall. Per the rubric, FDA Class II recalls involving significant injury or property damage reports, or structural defects, are rated Severe. Lack of sterility assurance in an injectable drug is a significant safety risk.
Plain-English summary
Anderson Compounding Pharmacy, Inc. is recalling 9 vials of HCG 11,000 Units, 30 mL Vial. The recall is being conducted because the product lacks sterility assurance. The affected product was distributed nationwide.
The recall includes all lots of the product. The source text does not specify a particular expiration date or lot number range beyond 'All Lots.'
Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- HCG 11,000 Units, 30 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
- Category
- Drug — Injectable
- Hazard
- Affected units
- 9
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)
- All Lots
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 68 recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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