Pharm D Solutions Recalls Glutathione Solution Due to Sterility Concerns
Pharm D Solutions is recalling 4,000 mL of Glutathione 200 mg/mL Solution because the product lacks assurance of sterility.
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, which corresponds to a Severe severity score under the rubric for significant injury or health risk potential.
Plain-English summary
Pharm D Solutions, LLC is recalling 4,000 milliliters of Glutathione 200 mg/mL Solution (NDC 69699-1504-30). The recall is being conducted because the product lacks assurance of sterility.
The affected product is identified by Lot 08012018:94 and has a discard-by date of 1/27/2019. 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
- Glutathione 200 mg/mL Solution, Pharm D Solutions, Houston, Texas --- NDC 69699-1504-30
- Manufacturer
- Pharm D Solutions, LLC
- Category
- Drug — Injectable Solution
- Hazard
- Affected units
- 4,000
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: 08012018:94 Discard by: 1/27/2019
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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