Severity
Moderate
CPSC recall · Reported May 24, 2017
The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock hazard.
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….
Sourced from official CPSC enforcement records. Verify recall #17747 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
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.
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
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.
The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock hazard.
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.
| 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.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported May 24, 2017.
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.
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).