FDA Drug Recalls

Recalls / Class I

Class ID-1501-2022

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

equate Magnesium Citrate, SALINE LAXATIVE, (1.745g/fl oz) 10 FL OZ (296mL), Grape Flavor, Distributed By: Walmart, Inc. Bentonville, AR 72716; NDC 49035-592-38 UPC 6 81131 28715 9

Affected lot / code info
Lot# 0525509, EXP 3/6/2023

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
18,324 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-1501-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.