FDA Drug Recalls

Recalls / Class I

Class ID-1510-2022

Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.

Product

Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Grape Flavor, 10 FL OZ (296 mL), Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015; NDC 0363-7162-38 UPC 3 11917 20159 7 (purple label).

Affected lot / code info
Lot # 0506255, EXP 10/24/2022

Why it was recalled

Microbial contamination of non-sterile products.

Recalling firm

Firm
Vi-Jon, LLC
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
1 Swan Dr, Smyrna, Tennessee 37167-2099

Distribution

Quantity
29,388 bottles
Distribution pattern
Distributed Nationwide in the USA as well as Canada and Panama.

Timeline

Recall initiated
2022-07-15
FDA classified
2022-09-09
Posted by FDA
2022-09-21
Terminated
2024-05-09
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1510-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class I recall: drug · FDA Drug Recalls