FDA Drug Recalls

Recalls / Class II

Class IID-0332-2017

Product

MIC Combo - Standard 15 mg/50 mg/100 mg/mL Injectable, 30 mL vials, 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: 03292016@5, 04122016@76, 04202016@5, 05182016@2, 06102016@2, 06282016@71, 09092016@1

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
308 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-0332-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.