Severity
Moderate
RSI Recalls Bathroom Medicine Cabinets Due to Injury Hazard; Sold Exclusively at The Home Depot
Reported: January 16, 2014 Initiated: January 16, 2014 #14082 About 14,000 units
RSI Home Products, of Anaheim, Calif. issued this CPSC recall on January 16, 2014. Classified as Moderate severity. Approximately About 14,000 units are affected. The recall was issued because: The mirror or its back panel can separate and fall out, posing an injury hazard to consumers.. 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 #14082) was formally reported on January 16, 2014. It is classified under Moderate severity, with a current status of Active. RSI Home Products, of Anaheim, Calif. is listed as the recalling firm. Federal records indicate About 14,000 units are affected.
The documented reason for this recall is: The mirror or its back panel can separate and fall out, posing an injury hazard to consumers. 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 stop using and uninstall the recalled bathroom medicine cabinet; and return it to The Home Depot for a full refund. — 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 6 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 12 years 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 14,000
Related Recalls
6
6 from same agency
Product Description
This recall involves four models of Glacier Bay®-branded bathroom medicine cabinets, manufactured between July 15, 2013 and October 10, 2013. They have a mirrored door, two adjustable and two fixed interior shelves. Some models have exterior display side shelves. They were sold in 21, 23 and 30-inch widths and in three finishes: cognac, java and white. "VOC" and the manufacture date are stamped on the exterior of the cabinet's back panel. The models below are included in this recall. The model and SKU number appear on the product's box. Model SKU Number Product Description S2327OS-ACO 1000004766 23" Swing Med Cab Open Side Cognac S3027OS-ACO 1000004797 30" Swing Med Cab Open Sides Cognac S2127C-JAV 1000004819 21" Curved Swing Med Cab Java S2127C-WHT 1000004822 21" Curved Swing Med Cab White
Reason for Recall
The mirror or its back panel can separate and fall out, posing an injury hazard to consumers.
Remedy
Consumers should immediately stop using and uninstall the recalled bathroom medicine cabinet; and return it to The Home Depot for a full refund.
Details
- Recalling Firm
- RSI Home Products, of Anaheim, Calif.
- Units Affected
- About 14,000
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 14082 |
| Date reported | January 16, 2014 |
| Date initiated | January 16, 2014 |
| Recalling firm | RSI Home Products, of Anaheim, Calif. |
| Units affected | About 14,000 |
| 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 four models of Glacier Bay®-branded bathroom medicine cabinets, manufactured between July 15, 2013 and October 10, 2013. They have a mirrored door, two adjustable and two fixed interior shelves. Some models have exterior display side shelves. They were sold in 21, 23 and 30-inch widths and in three finishes: cognac, java and white. "VOC" and the manufacture date are stamped on the exterior of the cabinet's back panel. The models below are included in this recall. The model and SKU number appear on the product's box. Model SKU Number Product Description S2327OS-ACO 1000004766 23" Swing Med Cab Open Side Cognac S3027OS-ACO 1000004797 30" Swing Med Cab Open Sides Cognac S2127C-JAV 1000004819 21" Curved Swing Med Cab Java S2127C-WHT 1000004822 21" Curved Swing Med Cab White. Recalled by RSI Home Products, of Anaheim, Calif.. Units affected: About 14,000.
Why was this product recalled? ▼
The mirror or its back panel can separate and fall out, posing an injury hazard to consumers.
What should consumers do? ▼
Consumers should immediately stop using and uninstall the recalled bathroom medicine cabinet; and return it to The Home Depot for a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on January 16, 2014. Severity: Moderate. Recall number: 14082.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (14082) 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).