Recalls / Class II
Class IID-0904-2018
Product
Phenylephrine HCL 50 mg in 0.9% Sodium Chloride 250 mL Bag (200 mcg/mL), SCA Pharmaceuticals, LLC, Windsor, CT
- Affected lot / code info
- Lot # 20180329@2, Exp 06/27/2018
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
- 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-0904-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.