Acme United Recalls PhysiciansCare Brand Allergy Relief and Cold and Cough Tablets Due to Failure to Meet Child Resis... — CPSC recall 23203

Published notice; closure not supplied

The CPSC record supplies a notice and remedy, not a current closure determination.

Source date May 18, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
This recall involves PhysiciansCare brand Allergy caplets with item number 90036, Allergy Plus tablets with item number 90091, and Cold and Cough tablets with item numbers 90092 and 90033. They are packaged in boxes of 50, 100 and 250 tablets/caplets. The item numbers are printed on the top right corner of the box. The recall includes the following: Item Number Description 90036 PhysiciansCare Allergy; 50 caplets 90091 PhysiciansCare Allergy Plus; 100 tablets Non-Drowsy Cold and Cough; 100 tablets 90033 PhysiciansCare Cold and Cough; 250 tablets
Reason
The recalled products contain diphenhydramine hydrochloride and acetaminophen which must be in child resistant packaging 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.
Classification
Not supplied
Recalling firm
Acme United, of Rocky Mount, North Carolina; Acme United, of Vancouver, Washington
Quantity
About 2,400
Agency-reported status
Published recall notice
Source record identifier
23203

Open the official record

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityRead the product description and official photos for model and lot identifiers.

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Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Last publish date
May 18, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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