Product Safety Recalls

Product Recall Tracker

MAGNESIUM CITRATE Recall D-1513-2022

Description: Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Grape Flavor, 10 FL OZ (296 mL), a) Best Choice UPC 0 70038 66220 4 Proudly Distributed By: Valu Merchandisers, Co. 5000 Kansas Ave Kansas City, KS 66106; b) CVS Health UPC 0 50428 30745 8 Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, CVS Health UPC 0 50428 32503 2 Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895; c) Equate NDC 49035-592-38 UPC 6 81131 28715 9 Distributed By: Walmart, Inc. Bentonville, AR 72716; d) HEB UPC 0 41220 51088 7 Made With Pride & Care For H-E-B San Antonio, TX 78204; Kroger UPC 0 41260 00871 9 Distributed By The Kroger Co. Cincinnati, Ohio 45202; e) Leader NDC 70000-0576-1 UPC 0 96295 14105 4 Distributed By Cardinal Health Dublin, Ohio 43017; f) Rexall UPC 0 72785 13417 1 Distributed By Dolgencorp, LLC 100 Mission Ridge Goodlettsville, TN 37072 USA, Rexall UPC 0 72785 13417 1 Distributed By Old East Main Co. 100 Mission Ridge Goodlettsville, TN 37072; g) Walgreens NDC 0363-7162-38 UPC 3 11917 20159 7 Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015 (purple label), Walgreens NDC 0363-7162-38 UPC 3 11917 20159 7 Distributed By: Walgreen Co. 200 Wilmot RD., Deerfield, IL 60015 (blue label)

MAGNESIUM CITRATE Recall D-1513-2022 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberD-1513-2022
Event ID90599
BrandMAGNESIUM CITRATE
Generic NameMAGNESIUM CITRATE
ManufacturerMAGNESIUM CITRATE
Original Package?1
Active SubstanceMAGNESIUM CITRATE
Drug RouteORAL
DistributionDistributed Nationwide in the USA as well as Canada and Panama.
Quantity8,064,834
Recall ReasonCGMP Deviations;
Drug ClassificationClass II
Drug Code Info20220921
Product NDC49035-592 70000-0576 0363-7162
Drug UPC0681131287159 070038662204 050428307458
Recall Initiation Date20220715
Report Date20220921
Classification Date20220909
Address1 Swan Dr
Smyrna, TN 37167-2099
United States
Recalling FirmVi-Jon, LLC
Initial Notification Press Release
Unique Ingredient IdentifierRHO26O1T9V
Drug Application Numberpart334
Structured Product Labeling (SPL ID)ee71cb44-834b-489a-af33-483d63b9ed80
Structured Product Labeling (SPL Set ID)a526d804-ac60-4251-90cc-da09af4dcd1c
Similar To

© 2021 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.