Pharm D Solutions Recalls Water for Injection Bags Due to Sterility Concerns
Pharm D Solutions is recalling 12 bags of Water Sterile for Injection due to a 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 and involves a lack of assurance of sterility in an injectable product, which poses a significant risk of serious injury or death if contaminated.
Plain-English summary
Pharm D Solutions, LLC is recalling 12 bags of Water Sterile for Injection 250 mL IV (NDC 69699-1407-25). The recall was initiated because of a lack of assurance of sterility for the product.
The affected product is identified by Lot 05222018 and has a discard by date of 10/21/2018. The recall is classified as Class II by the U.S. Food and Drug Administration.
The product was distributed nationwide. Consumers and healthcare providers should stop using the affected product and contact Pharm D Solutions, LLC for further instructions or a refund.
The recalled product
- Product
- Water Sterile for Injection 250 mL IV Pharm D Solutions, Houston, Texas --- NDC 69699-1407-25
- Manufacturer
- Pharm D Solutions, LLC
- Category
- Drug — IV Fluids
- Affected units
- 12
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: 05222018:12 Discard by: 10/21/2018
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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