D-0247-2016 Class II Terminated
FDA drug recall D-0247-2016 was initiated by US Compounding Inc on September 12, 2015 and is designated Class II. Reason for recall: Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an impact on sterility assurance. The recall status is terminated (terminated March 30, 2017). Affected quantity: 2,984 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- November 25, 2015
- Initiation Date
- September 12, 2015
- Termination Date
- March 30, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,984 bottles
Product Description
Dapiprazole (Diluent+Powder) 0.5% in 5 mL vial, For topical ophthalmic use, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-0201-99
Reason for Recall
Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an impact on sterility assurance.
Distribution Pattern
Nationwide
Code Information
Lot Numbers: 20150506@6 BUD: 11/28/2015; 20150805@40 BUD: 10/31/2015; 20151206@7 BUD: 12/5/2015; 20151704@21 BUD: 10/10/2015; 20152003@43 BUD: 9/12/2015