Severity
Moderate
Cabinet Health Recalls 4 oz. Refillable Medicine Bottles Due to Failure to Retain Child-Resistance; Risk of Child Poisoning
Reported: January 30, 2025 Initiated: January 30, 2025 #25110 About 65,000 units
Cabinet Health Inc., of Washington, D.C. issued this CPSC recall on January 30, 2025. Classified as Moderate severity. Approximately About 65,000 units are affected. The recall was issued because: The plastic lid's closure can degrade after repeated openings, causing the lid's child-resistance to diminish, posing a…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
Recall Insight
This CPSC action (record #25110) was formally reported on January 30, 2025. It is classified under Moderate severity, with a current status of Active. Cabinet Health Inc., of Washington, D.C. is listed as the recalling firm. Federal records indicate About 65,000 units are affected.
The documented reason for this recall is: The plastic lid's closure can degrade after repeated openings, causing the lid's child-resistance to diminish, posing a risk of poisoning, if the contents are swallowed by young children. 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 secure the recalled bottles out of the sight and reach of children and contact Cabinet Health for a free replacement lid. Consumers will be asked to submit a photo demons… — consumers holding this product should act on that instruction rather than relying on general guidance.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 1 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 1 year old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Recall Distribution by Severity Class
Units Affected
About 65,000
Related Recalls
6
1 from same agency
Product Description
This recall involves certain Cabinet Health 4 oz. Refillable Medicine Bottles with ABS plastic lids. The bottles are made of clear glass with blue, turquoise, orange or purple plastic lids labeled \"CABINET.\" Cabinet Health sold the bottles filled with over-the-counter drugs or as empty 4 oz. bottles. The recalled empty 4 oz. bottles were sold via cabinethealth.com from March 2023 through July 2024. Consumers with recalled empty bottles can identify them by the date of purchase. The recalled bottles filled with over-the-counter drugs have the following date codes on a sticker on the bottom of the bottle. Medication Name Lid Color Date Codes Tension Headache - Refillable Glass Bottle (Acetaminophen 500mg Caffeine 65mg) - 100 Count Blue 2029J07223 2029J07623 2029J07723 Allergy Relief - Refillable Glass Bottle (Diphenhydramine HCl 25mg) - 120 Count Turquoise 2265J07323 Pain Reliever and Nighttime Sleep Aid - Refillable Glass Bottle (Acetaminophen 500mg, Diphenhydramine 25mg) - 120 Count Blue 2127J06823 2127J23323 3040J23323 3051J23323 3051J23423Pain Reliever and Fever Reducer - Refillable Glass Bottle (Acetaminophen 500mg) - 120 Count Blue 2286J06323 2286J06523 2286J06623 2287J06623 2287J06723 Cough Relief - Refillable Glass Bottle (Dextromethorphan Hbr 15mg) - 60 Count Orange 2010J06923 2010J07023 3004J29623 3010J29623 3025J29623 Sleep Aid - Refillable Glass Bottle (Diphenhydramine HCl 50mg) - 70 Count Purple 3021J06823 3021J06923 3034J23423 3034J23523
Reason for Recall
The plastic lid's closure can degrade after repeated openings, causing the lid's child-resistance to diminish, posing a risk of poisoning, if the contents are swallowed by young children.
Remedy
Consumers should immediately secure the recalled bottles out of the sight and reach of children and contact Cabinet Health for a free replacement lid. Consumers will be asked to submit a photo demonstrating the destruction of the recalled lid. Cabinet Health and Amazon are contacting all known purchasers directly. This recall does not affect the medication within the bottles.
Details
- Recalling Firm
- Cabinet Health Inc., of Washington, D.C.
- Units Affected
- About 65,000
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 25110 |
| Date reported | January 30, 2025 |
| Date initiated | January 30, 2025 |
| Recalling firm | Cabinet Health Inc., of Washington, D.C. |
| Units affected | About 65,000 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
Frequently Asked Questions
What product was recalled? ▼
This recall involves certain Cabinet Health 4 oz. Refillable Medicine Bottles with ABS plastic lids. The bottles are made of clear glass with blue, turquoise, orange or purple plastic lids labeled \"CABINET.\" Cabinet Health sold the bottles filled with over-the-counter drugs or as empty 4 oz. bottles. The recalled empty 4 oz. bottles were sold via cabinethealth.com from March 2023 through July 2024. Consumers with recalled empty bottles can identify them by the date of purchase. The recalled bottles filled with over-the-counter drugs have the following date codes on a sticker on the bottom of the bottle. Medication Name Lid Color Date Codes Tension Headache - Refillable Glass Bottle (Acetaminophen 500mg Caffeine 65mg) - 100 Count Blue 2029J07223 2029J07623 2029J07723 Allergy Relief - Refillable Glass Bottle (Diphenhydramine HCl 25mg) - 120 Count Turquoise 2265J07323 Pain Reliever and Nighttime Sleep Aid - Refillable Glass Bottle (Acetaminophen 500mg, Diphenhydramine 25mg) - 120 Count Blue 2127J06823 2127J23323 3040J23323 3051J23323 3051J23423Pain Reliever and Fever Reducer - Refillable Glass Bottle (Acetaminophen 500mg) - 120 Count Blue 2286J06323 2286J06523 2286J06623 2287J06623 2287J06723 Cough Relief - Refillable Glass Bottle (Dextromethorphan Hbr 15mg) - 60 Count Orange 2010J06923 2010J07023 3004J29623 3010J29623 3025J29623 Sleep Aid - Refillable Glass Bottle (Diphenhydramine HCl 50mg) - 70 Count Purple 3021J06823 3021J06923 3034J23423 3034J23523. Recalled by Cabinet Health Inc., of Washington, D.C.. Units affected: About 65,000.
Why was this product recalled? ▼
The plastic lid's closure can degrade after repeated openings, causing the lid's child-resistance to diminish, posing a risk of poisoning, if the contents are swallowed by young children.
What should consumers do? ▼
Consumers should immediately secure the recalled bottles out of the sight and reach of children and contact Cabinet Health for a free replacement lid. Consumers will be asked to submit a photo demonstrating the destruction of the recalled lid. Cabinet Health and Amazon are contacting all known purchasers directly. This recall does not affect the medication within the bottles.
Which agency issued this recall? ▼
This recall was issued by the CPSC on January 30, 2025. Severity: Moderate. Recall number: 25110.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (25110) 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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Recall Context
Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
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Data Sources
Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
- Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- U.S. Census Bureau ACS — demographic + housing + income data. census.gov/programs-surveys/acs
- BLS Occupational Employment and Wage Statistics (OEWS) — wage + employment by occupation. bls.gov/oes
- BEA Regional Economic Accounts — GDP + personal income by state/metro. bea.gov/data/regional
- U.S. Census Bureau County Business Patterns — establishment + employment by industry. census.gov/cbp
- IRS Statistics of Income (SOI) — tax-return aggregate data. irs.gov/statistics
- data.gov — U.S. federal open-data portal — discovery layer for additional federal sources. data.gov
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).