DR®Power PRO XL501 Chipper Shredders
Summary
CPSC recall: DR®Power PRO XL501 Chipper Shredders. By Generac, of Waukesha, Wisconsin. Hazard: The fin scroll of the chipper shredder can fail, ejecting pieces of metal from the chipper shredder hopper during operation, posing a laceration hazard.. Remedy: Consumers should immediately stop using the recalled chipper shredders. DR Power Equipment is contacting all known purchasers and automatically sending them a repair kit with installation instructions. Consumers will also be provided with a sm
Details
Source
CPSC Consumer Product Recall
External ID
9553
Action Date
2023-03-02
Status
Recalled
Category
consumer_product
Product Description
This recall involves DR Power Chipper Shredder with model numbers CS35050BEN and CS35050BENR. The model number is on the
Context & Analysis
This is a unclassified recall.
This was one of 19 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Generac, of Waukesha, Wisconsin 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 (Generac, of Waukesha, Wisconsin) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Generac, of Waukesha, Wisconsin have FDA actions?
Generac, of Waukesha, Wisconsin 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 "9553" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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