FDA Drug Recalls

Recalls / Class II

Class IID-0405-2017

Product

Titan Up (INOS/CHOL/LEU/CAR/CHRO/LID) Injectable 25 mg/25 mg/1.5 mg/25 mg/0.025 mg/10 mg/mL, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL

Affected lot / code info
All lot codes of product prepared between 02/22/2016 and 09/14/2016, within expiry. Known lot code: 03252016@4, 04012016@9, 04042016@9, 04132016@14, 05062016@3, 06022016@7, 06152016@22, 06292016@25, 07282016@12.

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Wells Pharmacy Network LLC
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
1210 SW 33rd Ave, N/A, Ocala, Florida 34474-2853

Distribution

Quantity
433 vials
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-09-21
FDA classified
2017-01-04
Posted by FDA
2017-01-11
Terminated
2021-07-02
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0405-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.