Recalls / Class II
Class IID-0897-2018
Product
Diltiazem HCL 1 mg/mL in 125 mL 0.9% Sodium Chloride 100 mL bag (total volume 125 mL) (125 mg), SCA Pharmaceuticals, LLC, Windsor, CT
- Affected lot / code info
- Lot # 1218001315, 1218001316, 1218001349, 1218001416, 1218001510, 1218001682, 1218001683, 1218001684, 1218001721, 1218001763, 1218001764, Exp 07/26/2018-08/27/2018
Why it was recalled
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Recalling firm
- Firm
- SCA Pharmaceuticals, LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 755 Rainbow Rd Ste B, Windsor, Connecticut 06095-1024
Distribution
- Quantity
- 2,869 bags
- Distribution pattern
- Product was distributed throughout the United States.
Timeline
- Recall initiated
- 2018-06-14
- FDA classified
- 2018-07-02
- Posted by FDA
- 2018-07-11
- Terminated
- 2019-02-04
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0897-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.