Severity
Moderate
ModerateActive
CPSC recall · Reported June 10, 2010
IKEA Recalls Roller Blinds, all Roman Blinds and all Roll-Up Blinds Due to Risk of Strangulation
Roller Blinds: Strangulations can occur if the blind's looped bead chain is not attached to the wall or the floor with the tension device provided and a child's neck becomes entan…
Compiled from official public sources by the editorial team.
Verify with CPSC →
Ikea Home Furnishings, of Conshohocken, Pa. recalled This recall involves roller blinds that do not have a tension device attached to the bead… - a moderate-severity action.
IKEA Recalls Roller Blinds, all Roman Blinds and all Roll-Up Blinds Due to Risk of Strang… was recalled by Ikea Home Furnishings, of Conshohocken, Pa. in June 10, 2010. Reason: Roller Blinds: Strangulations can occur if the blind's looped bead chain is not attached to the wall or the f…. Remedy: Consumers should immediately stop using the roller blinds that do not have a tension devi…. Verify recall #10261 with the CPSC before acting.
The recall
Ikea Home Furnishings, of Conshohocken, Pa. issued this moderate-severity CPSC recall-Roller Blinds: Strangulations can occur if the blind's looped bead chain is not attached to the wall or the f….
- Moderate
- severity level
- June 10, 2010
- reported
Sourced from official CPSC enforcement records. Verify recall #10261 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #10261) was formally reported on June 10, 2010. It is classified under Moderate severity, with a current status of Active. Ikea Home Furnishings, of Conshohocken, Pa. is listed as the recalling firm. Federal records list the affected scope as About 3,360,000 (about 790,000 Roman blinds were recalled in November 2008 and August 2009 and about 533,000 Roller blinds were recalled in October 2009).
The documented reason for this recall is: Roller Blinds: Strangulations can occur if the blind's looped bead chain 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. Roman Bl… 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 the roller blinds that do not have a tension device attached to the chain, all Roman blinds and all roll-up blinds and return them to any IKEA store for a full… - 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, 3 from CPSC - 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.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices 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 3,360,000 (about 790,000 Roman blinds were recalled in November 2008 and August 2009 and about 533,000 Roller blinds were recalled in October 2009)
Related Recalls
6
3 from same agency
Product description
This recall involves roller blinds that do not have a tension device attached to the bead chain, all Roman blinds and all roll-up blinds.
Reason for recall
Roller Blinds: Strangulations can occur if the blind's looped bead chain 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. Roman Blinds: 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. An additional hazard exists when the Roman blind has a continuous looped bead chain that if not attached to the wall or floor, which poses a strangulation hazard to children. 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.
Remedy, what to do
Consumers should immediately stop using the roller blinds that do not have a tension device attached to the chain, all Roman blinds and all roll-up blinds and return them to any IKEA store for a full refund. In a previous recall, IKEA reminded consumers who have roller blinds with a tension device attached to the bead chain to make sure the tension device is installed into the wall or floor. If the consumer has difficulty installing the tension device, contact IKEA for additional information.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 10261 |
| Date reported | June 10, 2010 |
| Date initiated | June 10, 2010 |
| Recalling firm | Ikea Home Furnishings, of Conshohocken, Pa. |
| Affected scope | About 3,360,000 (about 790,000 Roman blinds were recalled in November 2008 and August 2009 and about 533,000 Roller blinds were recalled in October 2009) |
| 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 stop using the roller blinds that do not have a tension device attached to the chain, all Roman blin…
- Check the recall number (10261) 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 roller blinds that do not have a tension device attached to the bead chain, all Roman blinds and all roll-up blinds.. Recalled by Ikea Home Furnishings, of Conshohocken, Pa.. Units affected: About 3,360,000 (about 790,000 Roman blinds were recalled in November 2008 and August 2009 and about 533,000 Roller blinds were recalled in October 2009).
Why was this product recalled? ▼
Roller Blinds: Strangulations can occur if the blind's looped bead chain 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. Roman Blinds: 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. An additional hazard exists when the Roman blind has a continuous looped bead chain that if not attached to the wall or floor, which poses a strangulation hazard to children. 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.
What should consumers do? ▼
Consumers should immediately stop using the roller blinds that do not have a tension device attached to the chain, all Roman blinds and all roll-up blinds and return them to any IKEA store for a full refund. In a previous recall, IKEA reminded consumers who have roller blinds with a tension device attached to the bead chain to make sure the tension device is installed into the wall or floor. If the consumer has difficulty installing the tension device, contact IKEA for additional information.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 10, 2010. Severity: Moderate. Recall number: 10261.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (10261) 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.
CPSC Moderate
Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Serious Injury from Fire and Burn Hazards
· 2026-07-02
CPSC Moderate
Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury f…
· 2026-06-25
CPSC Moderate
Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by…
· 2026-06-18
FDA Devices Moderate
GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used i…
GE Medical Systems Information Technologies Inc · 2026-06-03
FDA Devices Critical
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit…
Medline Industries, LP · 2026-06-03
Compare this recall with Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Ser… →
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 10, 2010. 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.