RecallHawk

Bobcat & Steiner AirFX Finish Mower Deck attachments

Doosan Bobcat North America, of West Fargo, North Dakota

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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