Jacuzzi® Hot Tubs and Sundance® Spas
Summary
CPSC recall: Jacuzzi® Hot Tubs and Sundance® Spas. By Authorized Sundance Spas or Jacuzzi Hot Tubs dealers nationwide from July 2021 through December 2022 for between $6,500 and $30,000.. Hazard: The temperature sensor can relay incorrect water temperatures and cause the water to be hotter than the set temperature, posing injury (heat stroke) and thermal burn hazards.. Remedy: Consumers should use an accurate external thermometer to confirm the water temperature to be no higher than 104 degrees
Details
Source
CPSC Consumer Product Recall
External ID
9473
Action Date
2022-12-15
Status
Recalled
Category
consumer_product
Product Description
This recall involves JacuzziJ-200, J-300, J-400 and J-500 collection hot tubs and Sundance Spas 680, 780, 880 and 980 Se
Context & Analysis
This is a unclassified recall.
This was one of 14 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
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 (Authorized Sundance Spas or Jacuzzi Hot Tubs dealers nationwide from July 2021 through December 2022 for between $6,500 and $30,000.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Authorized Sundance Spas or Jacuzzi Hot Tubs dealers nationwide from July 2021 through December 2022 for between $6,500 and $30,000. have FDA actions?
This is the only FDA action we have on record for Authorized Sundance Spas or Jacuzzi Hot Tubs dealers nationwide from July 2021 through December 2022 for between $6,500 and $30,000. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9473" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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