FDA Drug Recalls

Recalls / Class II

Class IID-1211-2019

Product

Diltiazem 250 mg in NS 250 mL bag, Made by: Enterprise Pharmacy, 4400 Golf Acres Drive, Bldg. J Suite E, Charlotte, NC, 28208.

Affected lot / code info
Lots: EA161906 Exp. 4/16/2019; EA181906 Exp. 4/18/2019; EA231907 Exp. 4/23/2019; EA241907 Exp. 4/24/2019; EB061907 Exp. 5/7/2019; EB201907 Exp. 5/21/2019; EC181909 Exp. 6/16/2019

Why it was recalled

Lack of sterility assurance.

Recalling firm

Firm
CMC Enterprise Pharmacy
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
4400 Golf Acres Dr, N/A, Charlotte, North Carolina 28208-5968

Distribution

Quantity
1475 bags
Distribution pattern
NC

Timeline

Recall initiated
2019-04-12
FDA classified
2019-04-23
Posted by FDA
2019-05-01
Terminated
2019-10-30
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1211-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls