FDA Recalls Slenderella Compound Injectable Due to Sterility Concerns
Pharm D Solutions is recalling Slenderella Compound Injectable 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 drug recalls involving potential serious health consequences.
Plain-English summary
The U.S. Food and Drug Administration (FDA) has issued a recall for Slenderella Compound Injectable, manufactured by Pharm D Solutions, LLC in Houston, Texas. The recall is being conducted because the product lacks assurance of sterility.
The affected product is identified by NDC 69699-1617-30. The recall covers two specific lots: Lot 04202018:59 with a discard by date of 10/17/2018, and Lot 08282018:46 with a discard by date of 2/1/2019. The quantity involved is 5,000 milliliters.
The product was distributed nationwide. Consumers and healthcare providers should stop using the affected product and contact their pharmacist or the recalling firm for further instructions.
The recalled product
- Product
- Slenderella Compound Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1617-30
- Manufacturer
- Pharm D Solutions, LLC
- Category
- Drug — Injectable
- Hazard
- Affected units
- 5,000
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 (2)
- Lot: 04202018:59 Discard by: 10/17/2018
- 08282018:46 Discard by: 2/1/2019
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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