RecallHawk

Summary

CPSC recall: Kate and Laurel Astora and Valenti Mirrors. By Ningbo Zhenhai Tianen Photo Frame Manufacturing Co. Ltd., of China. Hazard: The recalled mirrors can detach from the frame, causing the mirror to fall, posing a laceration hazard to consumers.. Remedy: Consumers should immediately stop using the recalled mirrors and contact Uniek for instructions on how to remove and dispose of the mirror for a full refund. Consumers will be asked to email or text a photo of the properly disposed mirror

Details

Source

CPSC Consumer Product Recall

External ID

9644

Action Date

2023-06-08

Status

Recalled

Category

consumer_product

Product Description

This recall involves Kate and Laurel-branded Astora Capsule and Valenti Short Wood Arch mirrors. The oval-shaped Astora

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.

Ningbo Zhenhai Tianen Photo Frame Manufacturing Co. Ltd., of China 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 (Ningbo Zhenhai Tianen Photo Frame Manufacturing Co. Ltd., of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ningbo Zhenhai Tianen Photo Frame Manufacturing Co. Ltd., of China have FDA actions?

Ningbo Zhenhai Tianen Photo Frame Manufacturing Co. Ltd., of China 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 "9644" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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