Bugaboo Stroller Recall Issued Due to Risk of Handle Detaching

More than 50,000 Bugaboo baby strollers have been recalled, after dozens of reports were received that the carrying handles detached while in use, which may put babies in the strollers at risk of suffering a severe head trauma or other injury in a fall. 

A Bugaboo stroller recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on January 15, impacting the Bugaboo Cameleon and Bugboo Donkey models.

The manufacturer, Bugaboo Americas, of El Segundo, California, has received at least 58 reports that suggest the button on the stroller’s carry handle may disengage, causing the handle to detach and put children at serious risk of injury.

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 involves the carry handles on Bugaboo strollers with detachable carrycots/seats. The strollers consist of a base, sun canopy, and other various accessories sold in multiple colors. The recalled models have a fabric tag on the side of the sun canopy with the name “Bugaboo” and the model name.

The recalled Cameleon models have serial numbers ranging from 04011090900001 to 04031101009999, 08011090900001 to 08021100800386, and 140100093600531 to 140103123350418. The Donkey model serial number included in the recall ranges from 170101105300001 to 170104130900500. All serial numbers can be located on the stroller’s chassis, located under the carrycot/seat.

Both Donkey and Cameleon models were manufactured in China under Bugaboo International B.V., of Amsterdam, The Netherlands. The stroller’s were sold in the U.S. and Canada at Buy Buy Baby, Neiman Marcus, Nordstrom, Toys R Us and other baby product stores nationwide, online at Bugaboo.com and other retailers. The Donkey model was sold from January 2011 through December 2012 for between $1,200 and $1,600. The Cameleon model was sold between September 2009 and June 2012 for about $980.

Bugaboo International also recalled about 70,000 strollers and car seats in December of 2011, due to design defects that allowed infants to fall and suffer injuries. The Bugaboo car seat adapter recall was issued due to a defective car seat adaptor that failed to lock the seat in place. At least one injury was related to that recall. Another Bugaboo Bee stroller recall was issued in 2009 due to reports of the stroller’s swivel wheel locking while in motion, causing the stroller to tip over.

The CPSC recommends that consumers with the recalled “Cameleon” and “Donkey” model strollers stop using the product immediately and contact Bugaboo at (800) 460-2922 for a free replacement handle or visit their website at www.bugaboo.com and navigate to the link titled “Important Quality Initiative” for more information.

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 yesterday)

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 2 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 3 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.