Severity
Moderate
ModerateClass IIOngoing
FDA Drug recall · Reported July 3, 2024
Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233, Livonia, MI USA 48152, NDC 0904-6730-60, UPC Number 309046730606
Discoloration: Brownish tablets
Contract Pharmacal Corporation recalled Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARM… - a moderate-severity action.
Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARM… was recalled by Contract Pharmacal Corporation in July 3, 2024. Reason: Discoloration: Brownish tablets. Check the official notice for the remedy. Verify recall #D-0566-2024 with the FDA Drug before acting.
The recall
Contract Pharmacal Corporation issued this moderate-severity FDA Drug recall-Discoloration: Brownish tablets.
- Moderate
- severity level
- Class II
- classification
- July 3, 2024
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0566-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0566-2024) was formally reported on July 3, 2024, with the manufacturer initiating the action on May 20, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Contract Pharmacal Corporation is listed as the recalling firm, operating out of Hauppauge, NY. Federal records list the affected scope as 14,616 bottles.
The documented reason for this recall is: Discoloration: Brownish tablets Distribution data in the federal record shows the product reached: MI. 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, 5 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 - 14,287 drugs & medications 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.
Affected scope
14,616 bottles
Related Recalls
6
5 from same agency
Product description
Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233, Livonia, MI USA 48152, NDC 0904-6730-60, UPC Number 309046730606
Reason for recall
Discoloration: Brownish tablets
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0566-2024 |
| Date reported | July 3, 2024 |
| Date initiated | May 20, 2024 |
| Recalling firm | Contract Pharmacal Corporation |
| Firm location | Hauppauge, NY |
| Affected scope | 14,616 bottles |
| Distribution | MI |
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-0566-2024) 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? ▼
Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233, Livonia, MI USA 48152, NDC 0904-6730-60, UPC Number 309046730606. Recalled by Contract Pharmacal Corporation. Units affected: 14,616 bottles.
Why was this product recalled? ▼
Discoloration: Brownish tablets
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 3, 2024. Severity: Moderate. Recall number: D-0566-2024.
Where was the recalled product distributed? ▼
Distribution: MI.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0566-2024) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 July 3, 2024. 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.