Blue Ridge utility knives
Summary
CPSC recall: Blue Ridge utility knives. By Positec USA Inc., of Charlotte, North Carolina. Hazard: The recalled utility knife can become unlocked and the blade can protrude only while in the original packaging, posing a laceration hazard.. Remedy: Consumers should immediately and carefully inspect the packaging containing the Blue Ridge Utility Knife to determine whether the blade tip is protruding through the package. Carefully remove the knife from the packaging, avoiding the blade tip, and di
Details
Source
CPSC Consumer Product Recall
External ID
9620
Action Date
2023-05-11
Status
Recalled
Category
consumer_product
Product Description
This recall involves the Blue Ridge Utility Knife with a six-inch retractable blade. Model number BR922OU is printed on
Context & Analysis
This is a unclassified recall.
This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Positec USA Inc., of Charlotte, North Carolina 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 (Positec USA Inc., of Charlotte, North Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Positec USA Inc., of Charlotte, North Carolina have FDA actions?
Positec USA Inc., of Charlotte, North Carolina 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 "9620" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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