Severity
Critical
Vi-Jon, LLC issued this FDA Drug recall on September 21, 2022. Classified as Critical severity (Class I). Approximately 29,388 bottles units are affected. The recall was issued because: Microbial contamination of non-sterile products.. This recall notice is sourced from official FDA Drug enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
This FDA Drug action (record #D-1510-2022) was formally reported on September 21, 2022, with the manufacturer initiating the action on July 15, 2022. It is classified under Critical severity (Class I), with a current status of Terminated. Vi-Jon, LLC is listed as the recalling firm, operating out of Smyrna, TN. Federal records indicate 29,388 bottles units are affected.
The documented reason for this recall is: Microbial contamination of non-sterile products. Distribution data in the federal record shows the product reached: Distributed Nationwide in the USA as well as Canada and Panama.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 5 were also issued by FDA Drug. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 4 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Critical
Units Affected
29,388 bottles
Related Recalls
6
5 from same agency
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).
Microbial contamination of non-sterile products.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-1510-2022 |
| Date reported | September 21, 2022 |
| Date initiated | July 15, 2022 |
| Recalling firm | Vi-Jon, LLC |
| Units affected | 29,388 bottles |
| Distribution | Distributed Nationwide in the USA as well as Canada and Panama. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).