FDA Drug Recalls

Recalls / Class II

Class IID-0148-2016

Product

TRIMIX, injectable Solution, 20MG/1MG/20MCG/ML, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Affected lot / code info
t11242014@14, t10082014@1, t08152014@22, t08042014@31, t07252014@19, t07142015@19, t07102015@24, t07082014@2, t04142015@25, t04062015@16, t02242015@29, 12152014@9, 12032014@4, 11122014@2, 10292014@3, 10012014@15, 09232014@23, 09032014@3, 08132014@1, 06242015@4, 06172015@12, 06102015@5, 05272015@10, 05182015@6, 05132015@9, 05042015@5, 04222015@8, 03112015@4, 02102015@30, 01232015@6, 01072015@5;

Why it was recalled

Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

Recalling firm

Firm
JD & SN Inc., dba Moses Lake Professional Pharmacy
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
1555 Pilgrim St, N/A, Moses Lake, Washington 98837-4623

Distribution

Quantity
155 syringes
Distribution pattern
Nationwide

Timeline

Recall initiated
2015-07-24
FDA classified
2015-10-27
Posted by FDA
2015-11-04
Terminated
2016-04-13
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0148-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.