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CPSC recall · Reported March 17, 2022

Acme United Corporation Recalls PhysiciansCare Brand Over-the-Counter Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) which must be in child resistant packaging when being used in the househ…

Recall #
22733
Affected scope
About 165,000
Verify with CPSC →
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Acme United of Rocky Mount, North Carolina recalled This recall involves the PhysiciansCare brand Extra Strength Non Aspirin, Aspirin, Extra … - a moderate-severity action.

Acme United Corporation Recalls PhysiciansCare Brand Over-the-Counter Drugs Due to Failur… was recalled by Acme United of Rocky Mount, North Carolina in March 17, 2022. Reason: The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) wh…. Remedy: Consumers should immediately store the recalled products in a safe location out of reach …. Verify recall #22733 with the CPSC before acting.

The recall

Acme United of Rocky Mount, North Carolina issued this moderate-severity CPSC recall-The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) wh….

Moderate
severity level
March 17, 2022
reported

Sourced from official CPSC enforcement records. Verify recall #22733 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This CPSC action (record #22733) was formally reported on March 17, 2022. It is classified under Moderate severity, with a current status of Active. Acme United of Rocky Mount, North Carolina is listed as the recalling firm. Federal records list the affected scope as About 165,000.

The documented reason for this recall is: The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) which must be in child resistant packaging when being used in the household as required by the Poison Prevention… Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately store the recalled products in a safe location out of reach of children and contact Acme United for information on how to dispose of or return the product and receive a f… - consumers holding this product should act on that instruction rather than relying on general guidance.

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.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,287 drugs & medications recalls on record

-50005001,0001,5002,000 2006201220152018202120242026 263
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

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

About 165,000

Related Recalls

6

0 from same agency

Product description

This recall involves the PhysiciansCare brand Extra Strength Non Aspirin, Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack over-the-counter drugs. The products contain aspirin, acetaminophen, or ibuprofen. They are packaged in cardboard boxes of 50, 100, 250, and 500 tablets per box. Product Drug Tablet Amount Extra Strength Non Aspirin Acetaminophen (500 mg) 50 tablets 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Aspirin Aspirin (325 mg) 50 tablets 100 tablets 250 tablets 500 tablets Extra Strength Pain Reliever Acetaminophen (250 mg) Aspirin (250 mg) 100 tablets 250 tablets Ibuprofen Ibuprofen (200 mg) 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Medication Station / Multi-Pack Acetaminophen (500 mg) Aspirin (325 mg) Ibuprofen (200 mg) Antacid (420 mg) 4 boxes of 100 tablets each with outer station 4 boxes of 100 tablets each without outer station The Antacid is not subject to this recall.

Reason for recall

The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

Remedy, what to do

Consumers should immediately store the recalled products in a safe location out of reach of children and contact Acme United for information on how to dispose of or return the product and receive a full refund. Acme United is contacting all purchasers directly.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 22733
Date reported March 17, 2022
Date initiated March 17, 2022
Recalling firm Acme United of Rocky Mount, North Carolina
Affected scope About 165,000
Distribution Not disclosed
Official source CPSC notice →

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

What to do with this recall

Consumers should immediately store the recalled products in a safe location out of reach of children and contact Acme United for …

  • Check the recall number (22733) and product description against the item you own. Search the archive
  • Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official CPSC 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?
This recall involves the PhysiciansCare brand Extra Strength Non Aspirin, Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack over-the-counter drugs. The products contain aspirin, acetaminophen, or ibuprofen. They are packaged in cardboard boxes of 50, 100, 250, and 500 tablets per box. Product Drug Tablet Amount Extra Strength Non Aspirin Acetaminophen (500 mg) 50 tablets 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Aspirin Aspirin (325 mg) 50 tablets 100 tablets 250 tablets 500 tablets Extra Strength Pain Reliever Acetaminophen (250 mg) Aspirin (250 mg) 100 tablets 250 tablets Ibuprofen Ibuprofen (200 mg) 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Medication Station / Multi-Pack Acetaminophen (500 mg) Aspirin (325 mg) Ibuprofen (200 mg) Antacid (420 mg) 4 boxes of 100 tablets each with outer station 4 boxes of 100 tablets each without outer station The Antacid is not subject to this recall.. Recalled by Acme United of Rocky Mount, North Carolina. Units affected: About 165,000.
Why was this product recalled?
The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) which must be in child resistant packaging when being used in the household as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
What should consumers do?
Consumers should immediately store the recalled products in a safe location out of reach of children and contact Acme United for information on how to dispose of or return the product and receive a full refund. Acme United is contacting all purchasers directly.
Which agency issued this recall?
This recall was issued by the CPSC on March 17, 2022. Severity: Moderate. Recall number: 22733.
How do I check if my product is affected by a recall?
Check the product description and recall number (22733) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product?
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.

Nearby Recalls in This Category

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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: CPSC, reported March 17, 2022. 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.