Severity
Moderate
CPSC recall · Reported June 16, 2022
The recalled over-the-counter product contains the regulated substance acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act …
Sun Pharmaceutical Industries Inc., of Princeton, New Jersey recalled This recall involves the Kroger brand acetaminophen over-the-counter drug. The red, white… - a moderate-severity action.
Sun Pharma Recalls Kroger Brand Acetaminophen Due to Failure to Meet Child Resistant Pack… was recalled by Sun Pharmaceutical Industries Inc., of Princeton, New Jersey in June 16, 2022. Reason: The recalled over-the-counter product contains 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 #22162 with the CPSC before acting.
The recall
Sun Pharmaceutical Industries Inc., of Princeton, New Jersey issued this moderate-severity CPSC recall-The recalled over-the-counter product contains the regulated substance acetaminophen which must be in child r….
Sourced from official CPSC enforcement records. Verify recall #22162 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This CPSC action (record #22162) was formally reported on June 16, 2022. It is classified under Moderate severity, with a current status of Active. Sun Pharmaceutical Industries Inc., of Princeton, New Jersey is listed as the recalling firm. Federal records list the affected scope as About 34,660.
The documented reason for this recall is: The recalled over-the-counter product contains the regulated substance acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product 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 Kroger for information on how to properly dispose of the product and receive a … - 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.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
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 34,660
Related Recalls
6
0 from same agency
This recall involves the Kroger brand acetaminophen over-the-counter drug. The red, white and gray label states Kroger, Acetaminophen, Extended-Release Tablets USP, 650mg, Pain Reliever/Fever Reducer, 100 caplets. The bottle has a white continuous thread closure. The UPC number is 041260012877 with the batch codes AC45463, AC38213 or AC30682. The location of the UPC number is under the bar code on the packaging and the batch code is at the bottom of the label on the bottle.
The recalled over-the-counter product contains the regulated substance acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
Consumers should immediately store the recalled products in a safe location out of reach and sight of children. Contact Kroger for information on how to properly dispose of the product and receive a full refund.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 22162 |
| Date reported | June 16, 2022 |
| Date initiated | June 16, 2022 |
| Recalling firm | Sun Pharmaceutical Industries Inc., of Princeton, New Jersey |
| Affected scope | About 34,660 |
| 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 Kroger fo…
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.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
AbbVie Inc. · 2026-06-03
Llorens Pharmaceuticals International Division, Inc. · 2026-05-27
Safecor Health, LLC · 2026-05-27
IntegraDose Compounding Services LLC · 2026-05-27
Lupin Pharmaceuticals Inc. · 2026-05-27
Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
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.