Recalls / Class II
Class IID-1325-2019
Product
Human Chorionic Gonadotropin 5,000 IU vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
- Affected lot / code info
- Lot #: 01082019:88 Exp. 07/06/2019; 03182019:58 Exp. 09/14/2019
Why it was recalled
Lack of Sterility Assurance.
Recalling firm
- Firm
- Pharm D Solutions, LLC
- Notification channel
- Press Release
- Type
- FDA Mandated
- Address
- 1304 S Loop W, N/A, Houston, Texas 77054-4010
Distribution
- Quantity
- 279 vials
- Distribution pattern
- Nationwide within the United States
Timeline
- Recall initiated
- 2019-05-23
- FDA classified
- 2019-06-07
- Posted by FDA
- 2019-06-19
- Terminated
- 2021-02-05
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-1325-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.