Anderson Compounding Pharmacy Recalls Penicillin G Syringes Due to Sterility Concerns
Anderson Compounding Pharmacy is recalling Penicillin G 100,000/mL 10 mL Syringes because the product lacks sterility assurance. The recall covers all lots distributed nationwide.
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 recall is classified as FDA Class II. Per the rubric, FDA Class II recalls involving significant injury/property-damage reports or structural defects are rated Severe. Lack of sterility assurance in an injectable drug poses a significant risk of serious injury (infection/sepsis), fitting the Severe criteria for Class II drug recalls with potential for serious harm.
Plain-English summary
Anderson Compounding Pharmacy, Inc. is recalling Penicillin G 100,000/mL 10 mL Syringes. The recall is being conducted because the product lacks sterility assurance. The affected product is a 10 mL syringe containing Penicillin G at a concentration of 100,000/mL.
The recall includes all lots of the product. The distribution pattern is listed as nationwide. The recalling firm is Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy, located at 310 Bluff City Hwy, Bristol, TN.
Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for instructions on how to return or dispose of the medication. This recall is classified as Class II by the FDA.
The recalled product
- Product
- Penicillin G 100,000/mL 10 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
- Category
- Drug — Antibiotic
- Hazard
- Affected units
- 1
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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