Anderson Compounding Pharmacy Recalls Prostaglandin Tri-Mix Injection Due to Sterility Concerns
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix Injection nationwide due to a lack of 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 I or II recalls involving significant risks like sterility issues in injectable drugs are categorized as Severe (Score 4) when specific hospitalization reports are not explicitly detailed in the provided text but the defect is structural to the product's safety.
Plain-English summary
Anderson Compounding Pharmacy, Inc. is recalling Prostaglandin Tri-Mix 8.33:22.5:0.833 Injection, 2 mL Vials. The recall covers all lots of the product and is being conducted nationwide.
The recall was initiated because of a lack of sterility assurance for the medication. The source text does not specify the number of units affected or report any specific illnesses or injuries.
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
- Prostaglandin Tri-Mix 8.33:22.5:0.833 Injection, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
- Category
- Drug — Injectable Medication
- 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)
- 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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