Hart 18-Gauge 2" Brad Nailers
Techtronic Industries Vietnam Manufacturing Co., Ltd., of Vietnam
Summary
CPSC recall: Hart 18-Gauge 2" Brad Nailers. By Techtronic Industries Vietnam Manufacturing Co., Ltd., of Vietnam. Hazard: The contact sensor on the nailer can malfunction and involuntarily discharge a nail, posing a risk of serious injury to the user or bystanders.. Remedy: Consumers should immediately stop using the recalled nailer and return it to any Walmart USA store for a full refund. Consumers may also return items for free by mail via a scheduled pickup from your home. To schedule a free
Details
Source
CPSC Consumer Product Recall
External ID
9171
Action Date
2021-11-10
Status
Recalled
Category
consumer_product
Product Description
This recall involves Hart 18-Gauge 2" Brad Nailers with model numbers HPNR01, HPNR01B, HPNR01B-SK, or HPNR01BNCA. The wh
Context & Analysis
This is a unclassified recall.
This was one of 6 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Techtronic Industries Vietnam Manufacturing Co., Ltd., of Vietnam 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 (Techtronic Industries Vietnam Manufacturing Co., Ltd., of Vietnam) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Techtronic Industries Vietnam Manufacturing Co., Ltd., of Vietnam have FDA actions?
Techtronic Industries Vietnam Manufacturing Co., Ltd., of Vietnam 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 "9171" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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