Slenderella Compound Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1617-30
Reported: November 7, 2018 Initiated: September 10, 2018 #D-0186-2019
Product Description
Slenderella Compound Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1617-30
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- Pharm D Solutions, LLC
- Units Affected
- 5000 milliliters
- Distribution
- Nationwide
- Location
- Houston, TX
Frequently Asked Questions
What product was recalled? ▼
Slenderella Compound Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1617-30. Recalled by Pharm D Solutions, LLC. Units affected: 5000 milliliters.
Why was this product recalled? ▼
Lack of Assurance of Sterility
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 7, 2018. Severity: Moderate. Recall number: D-0186-2019.
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