Target Bunny Sippy Cup Recall Issued After Injury Reports

About 264,000 Target bunny sippy cups have been recalled from store shelves following reports that suggest the design may cause young children to suffer eye injuries from poking themselves with one of the ears. 

The Target sippy cup recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on April 26, after Target received at least six reports of incidents where children stuck themselves in the eye during normal use.

The problem appears to be with the rabbit shape of the cups, which include a pair of long, rigid ears. One of the ears points straight up and children can accidentally stick that part of the cup into their eye while trying to drink out of it, according to the CPSC.

Did You Know?

Ticketmaster Data Breach Impacts Millions of Customers

A massive Ticketmaster data breach exposed the names, addresses, phone numbers, credit card numbers and other personal information of more than 560 million customers, which have now been released on the dark web. Lawsuits are being pursued to obtain financial compensation.

Learn More

The recall affects two models of Target Home Bunny Sippy Cups, including a pink “female” cup with a model number of 200020683 and a blue “male” cup with a model number of 200020884. The model numbers are located on the bottom of the cups, which have handles on both sides and come with a white bunny head screw-on lid.

The recalled cups were sold exclusively at Target stores nationwide from February 2013 through April 5, 2012 for $3.

The CPSC recommends that consumers who have the cups stop using them immediately and return the cups to any target store for a full refund. Consumers with questions can call Target at (800) 444-0680 or can visit the company’s website at www.target.com.

0 Comments

Share Your Comments

I authorize the above comments be posted on this page*

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits
Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits (Posted 2 days ago)

A federal judge has agreed to divide lawsuits over gastroparesis injuries linked to drugs like Ozempic and Mounjaro into multiple phases, examining how the condition is diagnosed and whether plaintiffs' claims are preempted by federal laws.

Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn
Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn (Posted 3 days ago)

Lawsuit alleges that Abbott Laboratories failed to provide families and the medical community with adequate warnings about the risks associated with it’s cow’s milk-based Similac formula, which a now adult woman indicates has left her with life-long NEC injuries.

Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects
Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects (Posted 4 days ago)

Six breast cancer patients have asked a federal judge for permission to amend a complaint filed in March 2024, which describes problems linked to the device and painful side effects experienced when the tissue marker migrated out of position or shattered inside their bodies.