PlainRecalls
ModerateClass IITerminated

FDA Drug recall · Reported April 8, 2015

Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose)

Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules

Recall #
D-0430-2015
Affected scope
2284 cartons (100 individual unit doses per carton)
Initiated
January 6, 2015
Verify with FDA Drug →
View my saved recalls

American Health Packaging recalled Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed b… - a moderate-severity action.

Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed b… was recalled by American Health Packaging in April 8, 2015. Reason: Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules. Check the official notice for the remedy. Verify recall #D-0430-2015 with the FDA Drug before acting.

The recall

American Health Packaging issued this moderate-severity FDA Drug recall-Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules.

Moderate
severity level
Class II
classification
April 8, 2015
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0430-2015 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, 6 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.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,472 drugs & medications recalls on record

05001,0001,5002,000 2006201220152018202120242026 448
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

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 moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose)

Reason for recall

Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number D-0430-2015
Date reported April 8, 2015
Date initiated January 6, 2015
Recalling firm American Health Packaging
Firm location Columbus, OH
Affected scope 2284 cartons (100 individual unit doses per carton)
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.

  • Check the recall number (D-0430-2015) 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.

Frequently Asked Questions

What product was recalled?
Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose). Recalled by American Health Packaging. Units affected: 2284 cartons (100 individual unit doses per carton).
Why was this product recalled?
Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
Which agency issued this recall?
This recall was issued by the FDA Drug on April 8, 2015. Severity: Moderate. Recall number: D-0430-2015.
Where was the recalled product distributed?
Distribution: Nationwide.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

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 Drugs & Medications · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Compare this recall with Kian Pee Wan Capsules, 30-count bottles → · All Drugs & Medications recalls

This recall: FDA Drug, reported April 8, 2015. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026