Severity
Moderate
Strangulation Death of a Child Prompts Recall of Roman Shades, Roll-Up Blinds, and Roller Blinds by Hanover Direct/Domestications
Reported: November 10, 2010 Initiated: November 10, 2010 #11036 About 495,000 Roman shades and 28,500 roller/roll-up blinds (about 90,000 Roman shades were recalled in October 2009) units
CPSC recall on November 10, 2010. Classified as Moderate severity. Approximately About 495,000 Roman shades and 28,500 roller/roll-up blinds (about 90,000 Roman shades were recalled in October 2009) units are affected. The recall was issued because: Roman Shades: Strangulations can occur when a child places his/her neck between the exposed inner cord and the fabric o…. 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 #11036) was formally reported on November 10, 2010. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records indicate About 495,000 Roman shades and 28,500 roller/roll-up blinds (about 90,000 Roman shades were recalled in October 2009) units are affected, placing this recall in the million-unit bracket that typically triggers nationwide consumer alerts and retailer sweeps.
The documented reason for this recall is: Roman Shades: Strangulations can occur when a child places his/her neck between the exposed inner cord and the fabric on the backside of the blind or when a child pulls the cord out and wraps it around his/her neck. Rol… 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 all Roman shades with inner cords, all roll-up blinds, and all roller blinds that do not have a tension device, and contact the Window Covering Safety Council … — 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. 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 16 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 495,000 Roman shades and 28,500 roller/roll-up blinds (about 90,000 Roman shades were recalled in October 2009)
Related Recalls
6
0 from same agency
Product Description
This recall involves all styles of Roman shades with inner cords, all styles of roll-up blinds, and roller blinds that do not have a tension device. A tension device is intended to be attached to the continuous loop bead chain or continuous loop pull cord and installed into the wall or floor.
Reason for Recall
Roman Shades: Strangulations can occur when a child places his/her neck between the exposed inner cord and the fabric on the backside of the blind or when a child pulls the cord out and wraps it around his/her neck. Roll-up Blinds: Strangulations can occur if the lifting loops slide off the side of the blind and a child's neck becomes entangled on the free-standing loop or if a child places his/her neck between the lifting loop and the roll-up blind material. Roller Blinds: Strangulations can occur if the blind's continuous loop bead chain or continuous loop pull cord is not attached to the wall or the floor with the tension device provided and a child's neck becomes entangled in the free-standing loop.
Remedy
Consumers should immediately stop using all Roman shades with inner cords, all roll-up blinds, and all roller blinds that do not have a tension device, and contact the Window Covering Safety Council at (800) 506-4636 anytime for free repair kits or visit www.windowcoverings.org. Consumers who have roller blinds with a tension device should make sure the tension device is attached to the continuous loop bead chain or continuous loop pull cord and is installed into the wall or floor.
Details
- Units Affected
- About 495,000 Roman shades and 28,500 roller/roll-up blinds (about 90,000 Roman shades were recalled in October 2009)
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 11036 |
| Date reported | November 10, 2010 |
| Date initiated | November 10, 2010 |
| Recalling firm | Not disclosed |
| Units affected | About 495,000 Roman shades and 28,500 roller/roll-up blinds (about 90,000 Roman shades were recalled in October 2009) |
| 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 all styles of Roman shades with inner cords, all styles of roll-up blinds, and roller blinds that do not have a tension device. A tension device is intended to be attached to the continuous loop bead chain or continuous loop pull cord and installed into the wall or floor.. Units affected: About 495,000 Roman shades and 28,500 roller/roll-up blinds (about 90,000 Roman shades were recalled in October 2009).
Why was this product recalled? ▼
Roman Shades: Strangulations can occur when a child places his/her neck between the exposed inner cord and the fabric on the backside of the blind or when a child pulls the cord out and wraps it around his/her neck. Roll-up Blinds: Strangulations can occur if the lifting loops slide off the side of the blind and a child's neck becomes entangled on the free-standing loop or if a child places his/her neck between the lifting loop and the roll-up blind material. Roller Blinds: Strangulations can occur if the blind's continuous loop bead chain or continuous loop pull cord is not attached to the wall or the floor with the tension device provided and a child's neck becomes entangled in the free-standing loop.
What should consumers do? ▼
Consumers should immediately stop using all Roman shades with inner cords, all roll-up blinds, and all roller blinds that do not have a tension device, and contact the Window Covering Safety Council at (800) 506-4636 anytime for free repair kits or visit www.windowcoverings.org. Consumers who have roller blinds with a tension device should make sure the tension device is attached to the continuous loop bead chain or continuous loop pull cord and is installed into the wall or floor.
Which agency issued this recall? ▼
This recall was issued by the CPSC on November 10, 2010. Severity: Moderate. Recall number: 11036.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (11036) 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).