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CPSC recall · Reported June 16, 2022

Aurohealth Recalls Walgreens Brand Acetaminophen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

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 …

Recall #
22161
Affected scope
About 137,300
Verify with CPSC →
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Aurobindo Pharma Limited, of Telangana, India recalled This recall involves the Walgreens brand acetaminophen product. The red and white label s… - a moderate-severity action.

Aurohealth Recalls Walgreens Brand Acetaminophen Due to Failure to Meet Child Resistant P… was recalled by Aurobindo Pharma Limited, of Telangana, India in June 16, 2022. Reason: The recalled over-the-counter products contain the regulated substance acetaminophen which must be in child r…. Remedy: Consumers should immediately store the recalled products in a safe location out of reach …. Verify recall #22161 with the CPSC before acting.

The recall

Aurobindo Pharma Limited, of Telangana, India issued this moderate-severity CPSC recall-The recalled over-the-counter products contain the regulated substance acetaminophen which must be in child r….

Moderate
severity level
June 16, 2022
reported

Sourced from official CPSC enforcement records. Verify recall #22161 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This CPSC action (record #22161) was formally reported on June 16, 2022. It is classified under Moderate severity, with a current status of Active. Aurobindo Pharma Limited, of Telangana, India is listed as the recalling firm. Federal records list the affected scope as About 137,300.

The documented reason for this recall is: 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… 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 and sight of children. Contact Aurohealth for information on how to return the product at your nearest Walgree… - 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 137,300

Related Recalls

6

0 from same agency

Product description

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 for recall

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.

Remedy, what to do

Consumers should immediately store the recalled products in a safe location out of reach and sight of children. Contact Aurohealth for information on how to return the product at your nearest Walgreens store to receive a full refund.

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 22161
Date reported June 16, 2022
Date initiated June 16, 2022
Recalling firm Aurobindo Pharma Limited, of Telangana, India
Affected scope About 137,300
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 and sight of children. Contact Aurohealt…

  • Check the recall number (22161) 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 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.. Recalled by Aurobindo Pharma Limited, of Telangana, India. Units affected: About 137,300.
Why was this product recalled?
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.
What should consumers do?
Consumers should immediately store the recalled products in a safe location out of reach and sight of children. Contact Aurohealth for information on how to return the product at your nearest Walgreens store to receive a full refund.
Which agency issued this recall?
This recall was issued by the CPSC on June 16, 2022. Severity: Moderate. Recall number: 22161.
How do I check if my product is affected by a recall?
Check the product description and recall number (22161) 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.

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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 June 16, 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.