Aurohealth Recalls Walgreens Brand Acetaminophen Due to Failure to Meet Child Resistant Packaging Requirement; Risk o... — CPSC recall 22161

Published notice; closure not supplied

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

Source date Jun 16, 2022. 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 the Walgreens brand acetaminophen product. The red and white label states Walgreens, Easy Open for Adults, Pain Reliever, Acetaminophen, 500 mg, Fever Reducer, Extra Strength, 150 caplets. The bottle has a red continuous thread gear closure. UPC number 311917218090 and Lot numbers P2100627, P2100671, P2100672, P2100689 P2100747, P2100859 (each with expiration date Nov-2022) and P2200050 (with expiration date Jan-2023) are included in this recall. The UPC number, lot numbers and expiration date are printed near the drug facts panel on the label on the back of the bottle.
Reason
The recalled over-the-counter products contain the regulated substance 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
Aurobindo Pharma Limited, of Telangana, India; Aurohealth LLC, of East Windsor, New Jersey; Walgreen Co., of Deerfield, Illinois
Quantity
About 137,300
Agency-reported status
Published recall notice
Source record identifier
22161

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Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicability311917218090

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Not supplied

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

Dates in the source

Last publish date
Jun 16, 2022

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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