Stainless steel cable railing kits
Summary
CPSC recalled Stainless steel cable railing kits by Unknown Manufacturer. Hazard: The bottom hole on the cable support posts is over four inches from the bottom of the base plate, posing an entrapment hazard to consumers.. Remedy: Consumers should stop using the cable railing kits immediately, prevent children from accessing the area where they are located, and contact Vevor for a full refund. Vevor will provide pre-paid shipping labels so that consumers can return the recalled cable railing kits. Alternatively, consumers can provide photographic evidence of disposal or destruction of the cable support posts to recalling@vevor.com..
Details
Source
cpsc
External ID
25251
Action Date
2025-05-08
Status
Ongoing
Category
product
Product Description
This recall involves Vevor's cable railing kits for indoor or outdoor use. The cable support posts are made of stainless steel and were sold in black and silver colors. "Vevor" is printed on a label located on the top of each support post, and the P/N or P/C number is on the label of the product's outer packaging. If the consumer has discarded the outer packaging, the product model can be identified through the following product features. (P/N) or (P/C) # Color Number of Holes Overall Height of Cable Support Post (in inches) Cross-sectional Dimensions (in inches) Location of the Holes on Cable Support Post 1JZLGZHS9142UYBR4V0 black 10 36" 1.18" x 1.96" L-shaped Holes 1JZLGZHS1067CSWRBV0 black 12 42" 1.18" x 1.96" L-shaped Holes 1JZLGZ106755UOBB9V0 black 12 42" 1.96" x 1.96" L-shaped Holes LGZY106.72.55KZF0V0 silver 12 42" 1" x 2" Horizontal Holes 1JZLGZ91455YMDM3LV0 /1JZLGZ91455YMDM3LV0-0801 silver 10 36" 1.96" x 1.96" Horizontal Holes
Company
Context & Analysis
Unknown Manufacturer has 1320 FDA actions in our database.
Frequently Asked Questions
How often does Unknown Manufacturer have FDA actions?
Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls and 0 device clearances.
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The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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