PlainRecalls
CPSC Moderate Active

Halloween Pumpkin Decoration Kits Sold at Target Stores Recalled by Paper Magic Group Due to Choking Hazard

Reported: October 24, 2006 Initiated: October 24, 2006 #07013

Product Description

The recalled kits include plastic ears, eyes, noses, mouth, hands, shoes, hats, eyeglasses and jewelry that are used to decorate Halloween pumpkins. The recall includes Mr. Potato Head "Make a Monster Pumpkin" and "Make a Fireman Pumpkin" and Mrs. Potato Head "Make a Diva Pumpkin." The products are labeled for ages 2 and older. Products with small parts intended for children under 3 years old are prohibited due to a choking hazard.

Reason for Recall

The pumpkin decoration kits contain small parts that pose a choking hazard to young children.

Remedy

Consumers should stop using these pumpkin decorating kits immediately and return them to the nearest Target store for a full refund.

Details

Units Affected
About 97,000
Official Source
https://www.cpsc.gov/Recalls/2007/Halloween-Pumpkin-Decoration-Kits-Sold-at-Target-Stores-Recalled-by-Paper-Magic-Group-Due-to-Choking-Hazard

Frequently Asked Questions

What product was recalled? ▼
The recalled kits include plastic ears, eyes, noses, mouth, hands, shoes, hats, eyeglasses and jewelry that are used to decorate Halloween pumpkins. The recall includes Mr. Potato Head "Make a Monster Pumpkin" and "Make a Fireman Pumpkin" and Mrs. Potato Head "Make a Diva Pumpkin." The products are labeled for ages 2 and older. Products with small parts intended for children under 3 years old are prohibited due to a choking hazard.. Recalled by Paper Magic Group Inc., of Scranton, Pa.. Units affected: About 97,000.
Why was this product recalled? ▼
The pumpkin decoration kits contain small parts that pose a choking hazard to young children.
What should consumers do? ▼
Consumers should stop using these pumpkin decorating kits immediately and return them to the nearest Target store for a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on October 24, 2006. Severity: Moderate. Recall number: 07013.

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 →