Electric Kettles (ENFINIGY 1.5 l and ENFINIGY Pro 1.5 l)
ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany
Summary
CPSC recalled 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 for instructions on how to make the kettle unusable, which includes unplugging the kettle, cutting the cord, and uploading a photo of the product. Afterwards, consumers should safely dispose of the product..
Details
Source
cpsc
External ID
26489
Action Date
2026-05-14
Status
Ongoing
Category
product
Product Description
This recall involves ZWILLING J. A. Henckels Aktiengesellschaft Enfinigy Kettle (1.5 l) and Enfinigy Kettle Pro (1.5 l). The electric stainless-steel kettles come in various colors including black, silver, rose, gold, and pure-white. ZWILLING is silk printed on the kettle itself. Affected model numbers are: 53101-200, 53101-201 (1.5L ENFINIGY Electric Kettle); 53101-500, 53101-501, 53101-502, 53101-503, 53101-504 (1.5L ENFINIGY Electric Kettle Pro). The model numbers and "ZWILLING" can be found on the bottom of the kettle and the bottom of the power base.
Context & Analysis
ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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