Severity
Moderate
ModerateActive
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.
Rejuvenation Inc., of Portland, Ore., a division of Williams-Sonoma Inc., of San Francisco, Calif. recalled This recall involves Rejuvenation Cypress and Imbrie model articulated wall sconces. The … - a moderate-severity action.
Williams-Sonoma Recalls Rejuvenation Wall Sconces Due to Shock Hazard (Recall Alert) was recalled by Rejuvenation Inc., of Portland, Ore., a division of Williams-Sonoma Inc., of San Francisco, Calif. in May 24, 2017. Reason: The joint of the articulating arm can pinch or cut the electrical wire causing it to fray, posing a shock haz…. Remedy: Consumers should immediately stop using the recalled sconces and contact Rejuvenation for…. Verify recall #17747 with the CPSC before acting.
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
- 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 list the affected scope as About 1,055.
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.
Within the same product category the archive holds 6 closely related recalls, 6 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.
Household Products recalls over time
Where this recall sits in its category - 3,056 household products 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 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, what to 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.
Recall Profile
| 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. |
| Affected scope | About 1,055 |
| 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 sconces and contact Rejuvenation for instructions to receive a free repair o…
- Check the recall number (17747) 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 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.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 May 24, 2017. 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.