Acme United Corporation Recalls PhysiciansCare Brand Over-the-Counter Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
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What this record tells you
This CPSC record concerns Acme United Corporation Recalls PhysiciansCare Brand Over-the-Counter Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert) and names Acme United of Rocky Mount, North Carolina, Acme United of Vancouver, Washington as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.
- Firm: Acme United of Rocky Mount, North Carolina, Acme United of Vancouver, Washington
- Classification: The recalled over-the-counter products contain reg
- Status: Ongoing
- Recall date: 2022-03-17
Compare model, item/style number, serial range, manufacturing date, importer, retailer, color, and other physical identifiers listed in the notice.
A CPSC photograph may show only one variation, so use the model/serial information and remedy instructions as the stronger match.
Product Description & Identification
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 / Hazard Identified
Hazard: 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.. 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.
How to Check Whether Your Product Matches
A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.
- Confirm the full product and brand or recalling-firm name.
- Compare package size, color, flavor, model, style, or configuration when listed.
- Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
- Review the recall date and distribution information without assuming every seller is listed.
- Open the official CPSC source below and follow its current instructions.
If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.
Consumer Action Recorded in the Source
Distribution & Affected States
Nationwide retail and online distribution
Source-Provided Product Images
Image limitation: An image may show only one package, color, size, or model. Do not use a photograph alone to decide whether your product is affected.
Verify With the Issuing Agency
This record was last updated in our index on 2026-07-27 11:37:09 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.
Open CPSC Source Record →Record Transparency
- Issuing agency
- CPSC
- Source ID
- 9265
- Indexed update
- 2026-07-27 11:37:09 UTC
- Official source
- Open issuing-agency record