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CPSC recall · Reported November 3, 2015

Window Shades Recalled by Carra Imports Due to Strangulation Hazard (Recall Alert)

Cellular, Roller and Soft Horizontal Shades: Strangulation can occur when the shade's continuous loop pull cord or bead chain is not attached to the wall with a tension device and…

Recall #
16705
Affected scope
About 55,500
Verify with CPSC →
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The CPSC recalled This recall involves custom made-to-order cellular, roller, soft horizontal and Roman sty….

Window Shades Recalled by Carra Imports Due to Strangulation Hazard (Recall Alert) was recalled and listed by the CPSC in November 3, 2015. Reason: Cellular, Roller and Soft Horizontal Shades: Strangulation can occur when the shade's continuous loop pull co…. Remedy: Consumers should immediately stop using the recalled window shades and contact Carra for …. Verify recall #16705 with the CPSC before acting.

The recall

issued this CPSC recall-Cellular, Roller and Soft Horizontal Shades: Strangulation can occur when the shade's continuous loop pull co….

None
agency class
November 3, 2015
reported

Sourced from official CPSC enforcement records. Verify recall #16705 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. Consumers holding this product should act on the agency's documented remedy above 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.

Medical Devices recalls over time

Where this recall sits in its category - 41,021 medical devices recalls on record

01,0002,0003,0004,000 20052008201120142017202020232026 1,947

Product description

This recall involves custom made-to-order cellular, roller, soft horizontal and Roman style solar shades. The shades were sold in a variety of custom sizes and colors. The shades do not have any identifying labels or markings on the products.

Reason for recall

Cellular, Roller and Soft Horizontal Shades: Strangulation can occur when the shade's continuous loop pull cord or bead chain is not attached to the wall with a tension device and a child's neck becomes entangled in the free-standing loop. Roman Shades: Strangulation can occur when a child places his/her neck between the exposed inner cord and the fabric on the backside of the shade or when a child pulls the cord out and wraps it around his/her neck.

Remedy, what to do

Consumers should immediately stop using the recalled window shades and contact Carra for a free repair kit. If the recalled cellular, roller and soft horizontal shades do not have hold down devices installed, contact Carra Imports to receive a repair kit which includes a hold down device and instructions to install it. The repair kit for the Roman shades includes instructions to remove the pull cords and to install metal rings to raise and lower the shades to remove the hazard. Carra is directly contacting consumers who purchased the recalled window shades.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Not classified by agency
Status Active
Recall number 16705
Date reported November 3, 2015
Date initiated November 3, 2015
Recalling firm Not disclosed
Affected scope About 55,500
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 recalled window shades and contact Carra for a free repair kit. If the recalled cellu…

  • Check the recall number (16705) 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 custom made-to-order cellular, roller, soft horizontal and Roman style solar shades. The shades were sold in a variety of custom sizes and colors. The shades do not have any identifying labels or markings on the products.. Units affected: About 55,500.
Why was this product recalled?
Cellular, Roller and Soft Horizontal Shades: Strangulation can occur when the shade's continuous loop pull cord or bead chain is not attached to the wall with a tension device and a child's neck becomes entangled in the free-standing loop. Roman Shades: Strangulation can occur when a child places his/her neck between the exposed inner cord and the fabric on the backside of the shade or when a child pulls the cord out and wraps it around his/her neck.
What should consumers do?
Consumers should immediately stop using the recalled window shades and contact Carra for a free repair kit. If the recalled cellular, roller and soft horizontal shades do not have hold down devices installed, contact Carra Imports to receive a repair kit which includes a hold down device and instructions to install it. The repair kit for the Roman shades includes instructions to remove the pull cords and to install metal rings to raise and lower the shades to remove the hazard. Carra is directly contacting consumers who purchased the recalled window shades.
Which agency issued this recall?
This recall was issued by the CPSC on November 3, 2015. CPSC does not publish a hazard classification for this recall. Recall number: 16705.
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.

Nationwide recalls with similar severity or category timing

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Compare this recall with GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VS… → · All Medical Devices recalls

This recall: CPSC, reported November 3, 2015. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026