Bobcat & Steiner AirFX Finish Mower Deck attachments
Summary
CPSC recall: Bobcat & Steiner AirFX Finish Mower Deck attachments. By Doosan Bobcat North America, of West Fargo, North Dakota. Hazard: The recalled mower decks cannot be secured in the upright or tilted position by the locking pins during maintenance or service, posing a crush hazard.. Remedy: Consumers should immediately inspect and determine whether locking pins can be inserted while the deck is in the upright or tilted position during maintenance or service. Contact Doosan Bobcat North Ameri
Details
Source
CPSC Consumer Product Recall
External ID
10147
Action Date
2025-02-06
Status
Recalled
Category
consumer_product
Product Description
This recall involves Bobcat & Steiner AirFX Finish Mower Deck attachments. The mower decks are all black and labeled wit
Context & Analysis
This is a unclassified recall.
This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Doosan Bobcat North America, of West Fargo, North Dakota has 4 FDA actions in our database, including 2 recalls.
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 (Doosan Bobcat North America, of West Fargo, North Dakota) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Doosan Bobcat North America, of West Fargo, North Dakota have FDA actions?
Doosan Bobcat North America, of West Fargo, North Dakota has 4 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10147" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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