Prescription Labs Inc dba Greenpark: Drug Recall
Recall #D-0804-2021 · 08/18/2021
Class II: Risk
Recall Details
- Recall Number
- D-0804-2021
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Prescription Labs Inc dba Greenpark
- Status
- Terminated
- Date Initiated
- 08/18/2021
- Location
- Houston, TX, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 350 bottles
Reason for Recall
Lack of Assurance of Sterility
Product Description
Spironolactone Ophthalmic Solution 0.005 mg/mL, 15 mL bottles, Rx only, Greenpark Compounding Pharmacy
Distribution Pattern
Nationwide within the United States
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.