FDA Drug Recalls

Recalls / Class II

Class IID-0250-2020

Product

S-SODIUM SELINITE 0.219% INJ, 19ml glass vials, Rx only, Red Mountain Compounding Rx

Affected lot / code info
Lot #: S03062019JL@11, Exp 9/6/19; S04282019DH@05, Exp 10/28/19; S06182019DT@04, Exp 12/18/19; S06242019DH@11, Exp 12/24/19; " S07232019DH@15, Exp 1/23/20

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
6828 E Brown Rd Ste 101, N/A, Mesa, Arizona 85207-3761

Distribution

Quantity
11x10 ml glass vials
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2019-08-12
FDA classified
2019-11-05
Posted by FDA
2019-11-13
Terminated
2023-04-13
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0250-2020. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.