Severity
Moderate
ModerateActive
CPSC recall · Reported June 16, 2022
Time-Cap Labs Recalls Kroger Brand Aspirin and Ibuprofen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
The recalled over-the-counter products contain the regulated substances aspirin and ibuprofen which must be in child resistant packaging as required by the Poison Prevention Packa…
Compiled from official public sources by the editorial team.
Verify with CPSC →
The Kroger Co., of Cincinnati, Ohio recalled This recall involves the Kroger brand aspirin and ibuprofen over-the-counter drugs. For t… - a moderate-severity action.
Time-Cap Labs Recalls Kroger Brand Aspirin and Ibuprofen Due to Failure to Meet Child Res… was recalled by The Kroger Co., of Cincinnati, Ohio in June 16, 2022. Reason: The recalled over-the-counter products contain the regulated substances aspirin and ibuprofen which must be i…. Remedy: Consumers should immediately store the recalled products in a safe location out of reach …. Verify recall #22160 with the CPSC before acting.
The recall
The Kroger Co., of Cincinnati, Ohio issued this moderate-severity CPSC recall-The recalled over-the-counter products contain the regulated substances aspirin and ibuprofen which must be i….
- Moderate
- severity level
- June 16, 2022
- reported
Sourced from official CPSC enforcement records. Verify recall #22160 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #22160) was formally reported on June 16, 2022. It is classified under Moderate severity, with a current status of Active. The Kroger Co., of Cincinnati, Ohio is listed as the recalling firm. Federal records list the affected scope as About 209,430.
The documented reason for this recall is: The recalled over-the-counter products contain the regulated substances aspirin and ibuprofen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the pr… 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.
Drugs & Medications recalls over time
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.
Affected scope
About 209,430
Related Recalls
6
0 from same agency
Product description
This recall involves the Kroger brand aspirin and ibuprofen over-the-counter drugs. For the aspirin product, the green and yellow label states Kroger, Low Dose, Aspirin, 81 mg Delayed-Release Tablets / Pain Reliever, 300 enteric coated tablets. The bottle has a green continuous thread gear closure. For the ibuprofen product, the blue and white label states Kroger, Ibuprofen, Capsules, 200 mg Pain Reliever / Fever Reducer, 160 softgels. The bottle has a blue continuous thread gear closure. The following UPC and Lot numbers listed in the table are included in this recall and can be found on the label on the back of the bottle. Item UPC Lot numbers Aspirin 4126001295 A077J F032H F035H J011H K031H Ibuprofen 4126001298 FH1163 C11044 C11047 C11064 C11065 C11079 C11084
Reason for recall
The recalled over-the-counter products contain the regulated substances aspirin and ibuprofen 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 Kroger for information on how to properly dispose of the product and receive a full refund.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 22160 |
| Date reported | June 16, 2022 |
| Date initiated | June 16, 2022 |
| Recalling firm | The Kroger Co., of Cincinnati, Ohio |
| Affected scope | About 209,430 |
| 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…
- Check the recall number (22160) 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 Kroger brand aspirin and ibuprofen over-the-counter drugs. For the aspirin product, the green and yellow label states Kroger, Low Dose, Aspirin, 81 mg Delayed-Release Tablets / Pain Reliever, 300 enteric coated tablets. The bottle has a green continuous thread gear closure. For the ibuprofen product, the blue and white label states Kroger, Ibuprofen, Capsules, 200 mg Pain Reliever / Fever Reducer, 160 softgels. The bottle has a blue continuous thread gear closure. The following UPC and Lot numbers listed in the table are included in this recall and can be found on the label on the back of the bottle. Item UPC Lot numbers Aspirin 4126001295 A077J F032H F035H J011H K031H Ibuprofen 4126001298 FH1163 C11044 C11047 C11064 C11065 C11079 C11084. Recalled by The Kroger Co., of Cincinnati, Ohio. Units affected: About 209,430.
Why was this product recalled? ▼
The recalled over-the-counter products contain the regulated substances aspirin and ibuprofen 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 Kroger for information on how to properly dispose of the product and receive a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 16, 2022. Severity: Moderate. Recall number: 22160.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (22160) 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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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.