Severity
Moderate
FDA Drug recall · Reported January 15, 2014
Presence of Foreign Substance; metal particulates were visually observed in the tablets.
Watson Laboratories Inc recalled Carisoprodol Tablets, USP, CIV, 350 mg, 500 count bottle, Rx only. Manufactured by Watson… - a moderate-severity action.
Carisoprodol Tablets, USP, CIV, 350 mg, 500 count bottle, Rx only. Manufactured by Watson… was recalled by Watson Laboratories Inc in January 15, 2014. Reason: Presence of Foreign Substance; metal particulates were visually observed in the tablets.. Check the official notice for the remedy. Verify recall #D-397-2014 with the FDA Drug before acting.
The recall
Watson Laboratories Inc issued this moderate-severity FDA Drug recall-Presence of Foreign Substance; metal particulates were visually observed in the tablets..
Sourced from official FDA Drug enforcement records. Verify recall #D-397-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-397-2014) was formally reported on January 15, 2014, with the manufacturer initiating the action on December 23, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Watson Laboratories Inc is listed as the recalling firm, operating out of Corona, CA. Federal records list the affected scope as 4,439 bottles.
The documented reason for this recall is: Presence of Foreign Substance; metal particulates were visually observed in the tablets. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
4,439 bottles
Related Recalls
6
0 from same agency
Carisoprodol Tablets, USP, CIV, 350 mg, 500 count bottle, Rx only. Manufactured by Watson Pharma Private Ltd, Verna, Salcette, Goa, 403 722 INDIA. Distributed by: Watson Pharma Ltd, Parsippany, NJ 07054. NDC 0591-5513-05.
Presence of Foreign Substance; metal particulates were visually observed in the tablets.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-397-2014 |
| Date reported | January 15, 2014 |
| Date initiated | December 23, 2013 |
| Recalling firm | Watson Laboratories Inc |
| Firm location | Corona, CA |
| Affected scope | 4,439 bottles |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported January 15, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.