PlainRecalls
CPSC Moderate Active

Bugaboo Car Seat Adapter Recalled Due to Fall Hazard

Reported: December 22, 2011 Initiated: December 22, 2011 #12067

Product Description

This recall involves the Bugaboo car seat adapter models 80400GC01 and 80401GC02. The adapters are devices designed to attach car seats to stroller frames. They are made of silver aluminum tubing and black plastic connecting parts.

Reason for Recall

When the adapter is used on a stroller that also has a wheeled board accessory attached for transporting a standing toddler, and the car seat is positioned so the child faces forward, the car seat can disconnect from the adapter and fall.

Remedy

Consumers should immediately stop using the adapter and contact Bugaboo for a free service kit and decals.

Details

Units Affected
About 64,000
Official Source
https://www.cpsc.gov/Recalls/2012/Bugaboo-Car-Seat-Adapter-Recalled-Due-to-Fall-Hazard

Frequently Asked Questions

What product was recalled? ▼
This recall involves the Bugaboo car seat adapter models 80400GC01 and 80401GC02. The adapters are devices designed to attach car seats to stroller frames. They are made of silver aluminum tubing and black plastic connecting parts.. Units affected: About 64,000.
Why was this product recalled? ▼
When the adapter is used on a stroller that also has a wheeled board accessory attached for transporting a standing toddler, and the car seat is positioned so the child faces forward, the car seat can disconnect from the adapter and fall.
What should consumers do? ▼
Consumers should immediately stop using the adapter and contact Bugaboo for a free service kit and decals.
Which agency issued this recall? ▼
This recall was issued by the CPSC on December 22, 2011. Severity: Moderate. Recall number: 12067.

Related Recalls

FDA Devices Moderate

Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…

Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…

Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate

Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…

Fujirebio Diagnostics, Inc. · 2026-02-11

Explore Related Data

Vehicle Safety → Drug Information →