Ashland 10-inch and 14-inch two-bar casement window hinge tracks
Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas
Summary
CPSC recall: Ashland 10-inch and 14-inch two-bar casement window hinge tracks. By Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas. Hazard: The metal sliding arm can disengage from the hinge track causing the window sash to fall, posing an impact injury hazard to consumers.. Remedy: Consumers should leave windows in the closed and locked positions and immediately contact AmesburyTruth to coordinate a free window inspection by a professional, who will install free replacement hing
Details
Source
CPSC Consumer Product Recall
External ID
10229
Action Date
2025-04-03
Status
Recalled
Category
consumer_product
Product Description
This recall involves Ashland 10-inch and 14-inch two-bar right-hand and left-hand casement window hinge tracks installed
Context & Analysis
This is a unclassified recall.
This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas 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 (Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas have FDA actions?
Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas 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 "10229" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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