Electric Kettles (ENFINIGY 1.5 l and ENFINIGY Pro 1.5 l)
ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany
Summary
CPSC recall: Electric Kettles (ENFINIGY 1.5 l and ENFINIGY Pro 1.5 l). By ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany. Hazard: The kettle's handle can loosen and separate from the kettle, causing hot contents to spill, posing a risk of serious injury due to a burn hazard.. Remedy: Consumers should stop using the recalled kettles immediately and contact ZWILLING J. A. Henckels Aktiengesellschaft for a full refund. Consumers in the U.S. should visit www.zwilling.com/kettle-recall
Details
Source
CPSC Consumer Product Recall
External ID
10776
Action Date
2026-05-14
Status
Recalled
Category
consumer_product
Product Description
This recall involves ZWILLING J. A. Henckels Aktiengesellschaft Enfinigy Kettle (1.5 l) and Enfinigy Kettle Pro (1.5 l).
Context & Analysis
This is a unclassified recall.
This was one of 24 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany have FDA actions?
ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10776" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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