LiCB CR2032 3V Lithium Coin Batteries
Guangzhou Lichengbei Battery Technology Co., Ltd., dba LiCB, of China
Summary
CPSC recall: LiCB CR2032 3V Lithium Coin Batteries. By Guangzhou Lichengbei Battery Technology Co., Ltd., dba LiCB, of China. Hazard: The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under?Reese's Law.?When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.. Remedy: Consumers should stop using the coin batteries immediately, place them in an area that child
Details
Source
CPSC Consumer Product Recall
External ID
10771
Action Date
2026-05-14
Status
Recalled
Category
consumer_product
Product Description
This recall involves LiCB-branded lithium coin batteries. The three-volt silver batteries were sold in packs of two, eac
Context & Analysis
This is a unclassified recall.
This was one of 24 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Guangzhou Lichengbei Battery Technology Co., Ltd., dba LiCB, 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 (Guangzhou Lichengbei Battery Technology Co., Ltd., dba LiCB, 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 Guangzhou Lichengbei Battery Technology Co., Ltd., dba LiCB, of China have FDA actions?
Guangzhou Lichengbei Battery Technology Co., Ltd., dba LiCB, 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 "10771" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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