Ceiling Hoists with Straps
Summary
CPSC recall: Ceiling Hoists with Straps. By REI and various other independent stores, and online at Amazon.com and designbydelta.com from February 2017 through July 2024 for about $40.. Hazard: The plastic buckles on the straps being used to hold a kayak, canoe or other large objects with the ceiling hoist can break, posing an injury hazard to consumers.. Remedy: Consumers should immediately stop using the Ceiling Hoist with Straps and contact Delta Cycle Corp to receive free replacement straps.
Details
Source
CPSC Consumer Product Recall
External ID
10043
Action Date
2024-09-05
Status
Recalled
Category
consumer_product
Product Description
This recall involves Ceiling Hoists with Straps with model number RS2300. The model number is only listed on the product
Context & Analysis
This is a unclassified recall.
This was one of 4 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 (REI and various other independent stores, and online at Amazon.com and designbydelta.com from February 2017 through July 2024 for about $40.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does REI and various other independent stores, and online at Amazon.com and designbydelta.com from February 2017 through July 2024 for about $40. have FDA actions?
This is the only FDA action we have on record for REI and various other independent stores, and online at Amazon.com and designbydelta.com from February 2017 through July 2024 for about $40. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10043" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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