FDA Drug recall · Reported August 6, 2014
Cardura XL (doxazosin mesylate extended release tablets, 4 mg, 30-count bottle, Rx only, Distributed by Roerig Division of Pfizer Inc., New York, NY 10017, NDC 0049-2710-30
Failed Impurities/Degradation Specifications: Product from this lot may not meet specifications for a product degradant.
Pfizer Inc. recalled Cardura XL (doxazosin mesylate extended release tablets, 4 mg, 30-count bottle, Rx only, … - a low-severity action.
Cardura XL (doxazosin mesylate extended release tablets, 4 mg, 30-count bottle, Rx only, … was recalled by Pfizer Inc. in August 6, 2014. Reason: Failed Impurities/Degradation Specifications: Product from this lot may not meet specifications for a product…. Check the official notice for the remedy. Verify recall #D-1485-2014 with the FDA Drug before acting.
The recall
Pfizer Inc. issued this low-severity FDA Drug recall-Failed Impurities/Degradation Specifications: Product from this lot may not meet specifications for a product….
- Low
- severity level
- Class III
- classification
- August 6, 2014
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1485-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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, 1 from FDA Drug - 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,781 children & baby products recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.
Product description
Cardura XL (doxazosin mesylate extended release tablets, 4 mg, 30-count bottle, Rx only, Distributed by Roerig Division of Pfizer Inc., New York, NY 10017, NDC 0049-2710-30
Reason for recall
Failed Impurities/Degradation Specifications: Product from this lot may not meet specifications for a product degradant.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-1485-2014 |
| Date reported | August 6, 2014 |
| Date initiated | June 19, 2014 |
| Recalling firm | Pfizer Inc. |
| Firm location | New York, NY |
| Affected scope | 22,461 bottles |
| Distribution | Nationwide (Continental USA and Puerto Rico). A portion of the bulk lot was supplied to Pfizer Germany for packaging into blisters for non- USA market. One of these lots in Germany was placed in stability having acceptable results, there… |
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.
- Check the recall number (D-1485-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
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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Nationwide recalls with similar severity or category timing
Drug and device notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Low), closest by report date among other firms and states.
Similar Children & Baby Products · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Compare this recall with CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per … → · All Children & Baby Products recalls
Methodology · Corrections · Archive as of August 2026