Pharm D Solutions Recalls Beta-Complex Injectable Due to Sterility Concerns
Pharm D Solutions is recalling Beta-complex B-1, B-6, B-3, B-12, B-5 100, 2.54 Injectable due to lack of assurance of sterility. The product was 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. According to the rubric, an FDA Class II recall involving a significant hazard (lack of sterility in an injectable) corresponds to a severity score of 4 (Severe), particularly given the potential for serious injury from non-sterile injectables.
Plain-English summary
Pharm D Solutions, LLC is recalling Beta-complex B-1, B-6, B-3, B-12, B-5 100, 2.54 Injectable (NDC 69699-1611-30). The recall was initiated because of a lack of assurance of sterility for the product.
The affected product is a 6000 milliliter injectable solution. The specific lot number is 06182018:55, with a discard by date of 12/25/2018. The product was distributed nationwide.
Consumers and healthcare providers should stop using the recalled product and contact Pharm D Solutions, LLC for further instructions or a refund.
The recalled product
- Product
- Beta-complex B-1, B-6, B-3, B-12, B-5 100, 2.54 Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1611-30
- Manufacturer
- Pharm D Solutions, LLC
- Category
- Drug — Injectable
- Affected units
- 6,000
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)
- Lot: 06182018:55 Discard by: 12/25/2018
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 79 recalled by Pharm D Solutions, LLC 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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