Severity
Low
FDA Drug recall · Reported January 29, 2014
Failed Stability Specifications: this product is below specification for preservative content.
Teva Pharmaceuticals USA, Inc. recalled Fluconazole Oral Suspension, 10 mg/mL, 35 ml bottle, RX only, Mfd by Cipla, Ltd., Goa, In… - a low-severity action.
Fluconazole Oral Suspension, 10 mg/mL, 35 ml bottle, RX only, Mfd by Cipla, Ltd., Goa, In… was recalled by Teva Pharmaceuticals USA, Inc. in January 29, 2014. Reason: Failed Stability Specifications: this product is below specification for preservative content.. Check the official notice for the remedy. Verify recall #D-747-2014 with the FDA Drug before acting.
The recall
Teva Pharmaceuticals USA, Inc. issued this low-severity FDA Drug recall-Failed Stability Specifications: this product is below specification for preservative content..
Sourced from official FDA Drug enforcement records. Verify recall #D-747-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-747-2014) was formally reported on January 29, 2014, with the manufacturer initiating the action on November 14, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Teva Pharmaceuticals USA, Inc. is listed as the recalling firm, operating out of Sellersville, PA. Federal records list the affected scope as 234,242 bottles.
The documented reason for this recall is: Failed Stability Specifications: this product is below specification for preservative content. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
234,242 bottles
Related Recalls
6
0 from same agency
Fluconazole Oral Suspension, 10 mg/mL, 35 ml bottle, RX only, Mfd by Cipla, Ltd., Goa, India, Dist by Teva Pharmaceuticals USA, Inc., Sellersville, PA. NDC: 0093-5414-95.
Failed Stability Specifications: this product is below specification for preservative content.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-747-2014 |
| Date reported | January 29, 2014 |
| Date initiated | November 14, 2013 |
| Recalling firm | Teva Pharmaceuticals USA, Inc. |
| Firm location | Sellersville, PA |
| Affected scope | 234,242 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 29, 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.