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CPSC recall · Reported May 24, 2017

Williams-Sonoma Recalls Rejuvenation Wall Sconces Due to Shock Hazard (Recall Alert)

The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock hazard.

Recall #
17747
Units affected
About 1,055
Verify with CPSC →

The recall

Rejuvenation Inc., of Portland, Ore., a division of Williams-Sonoma Inc., of San Francisco, Calif. issued this moderate-severity CPSC recall — The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock haz….

Moderate
severity level
About 1,055
units affected
May 24, 2017
reported

Sourced from official CPSC enforcement records. Verify recall #17747 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This CPSC action (record #17747) was formally reported on May 24, 2017. It is classified under Moderate severity, with a current status of Active. Rejuvenation Inc., of Portland, Ore., a division of Williams-Sonoma Inc., of San Francisco, Calif. is listed as the recalling firm. Federal records indicate About 1,055 units are affected.

The documented reason for this recall is: The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock hazard. 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 recalled sconces and contact Rejuvenation for instructions to receive a free repair or replacement sconce, including shipping and charges for inspecting, r… — 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 and NHTSA 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 9 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.

Where this recall sits in the database

Severity2119858883High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.

Severity

Moderate

Units Affected

About 1,055

Related Recalls

6

6 from same agency

Product Description

This recall involves Rejuvenation Cypress and Imbrie model articulated wall sconces. The wall sconces have articulating jointed arms and adjustable shades in various colors and finishes. They were sold in plug-in (also called pin-up) and hard wired versions. The sconce arms measure about 16 inches long. Each sconce has a label located inside the canopy of the sconce that contains the SKU number, configuration ID, manufacturing date and production order number. The following SKU numbers are included in the recall and are printed on the production label: A1327, A1328, A1329, A1330, A1331, A1332, A9591, A9592, A9593, A9594, A9595, A9596, A3621, A3622, A3625, A3626, A3623, A3624.

Reason for Recall

The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock hazard.

Remedy

Consumers should immediately stop using the recalled sconces and contact Rejuvenation for instructions to receive a free repair or replacement sconce, including shipping and charges for inspecting, removing and replacing the lamps by using a licensed electrician. Rejuvenation is contacting consumers who purchased the recalled sconces directly.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 17747
Date reported May 24, 2017
Date initiated May 24, 2017
Recalling firm Rejuvenation Inc., of Portland, Ore., a division of Williams-Sonoma Inc., of San Francisco, Calif.
Units affected About 1,055
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 1,055 units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

Frequently Asked Questions

What product was recalled?
This recall involves Rejuvenation Cypress and Imbrie model articulated wall sconces. The wall sconces have articulating jointed arms and adjustable shades in various colors and finishes. They were sold in plug-in (also called pin-up) and hard wired versions. The sconce arms measure about 16 inches long. Each sconce has a label located inside the canopy of the sconce that contains the SKU number, configuration ID, manufacturing date and production order number. The following SKU numbers are included in the recall and are printed on the production label: A1327, A1328, A1329, A1330, A1331, A1332, A9591, A9592, A9593, A9594, A9595, A9596, A3621, A3622, A3625, A3626, A3623, A3624.. Recalled by Rejuvenation Inc., of Portland, Ore., a division of Williams-Sonoma Inc., of San Francisco, Calif.. Units affected: About 1,055.
Why was this product recalled?
The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock hazard.
What should consumers do?
Consumers should immediately stop using the recalled sconces and contact Rejuvenation for instructions to receive a free repair or replacement sconce, including shipping and charges for inspecting, removing and replacing the lamps by using a licensed electrician. Rejuvenation is contacting consumers who purchased the recalled sconces directly.
Which agency issued this recall?
This recall was issued by the CPSC on May 24, 2017. Severity: Moderate. Recall number: 17747.
How do I check if my product is affected by a recall?
Check the product description and recall number (17747) 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.

Compare this recall with Electrolux Group Recalls Frigidaire Gas Ranges Due to Burn … →

Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported May 24, 2017.

  • 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)

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.

Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).