Z-1313-2014Class II

Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco the Monkey". Non-Fluid Filled Teething Ring

Name: Z-1313-2014 Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco the Monkey". Non-Fluid Filled Teething Ring
Creator: Infantino LLC
Published: 2014-01-06
License: https://open.fda.gov/license/

Infantino LLC / initiated 2014-01-06 / Terminated

FDA source

Infantino LLC began a recall of Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco the Monkey". Non-Fluid Filled Teething Ring on 2014-01-06. FDA classified it as Class II and gives the reason as "Infantino initiated this voluntary recall of all lots of Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teethe Coco the Monkey", Model Number 206-647, because the tail of the monkey may pose a choking hazard to...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1313-2014
Classification: Class II
Status: Terminated
Initiated: 2014-01-06
Posted: 2014-04-01
Terminated: 2015-04-23
Recalling firm: Infantino LLC
Product: Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco the Monkey". Non-Fluid Filled Teething Ring.
Product code: MEF Ring, Teething, Non-Fluid Filled
Reason for recall: Infantino initiated this voluntary recall of all lots of Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teethe Coco the Monkey", Model Number 206-647, because the tail of the monkey may pose a choking hazard to young children.
FDA root cause: Other
Action: Infantino, LLC initiated this recall by notifying its customer on January 6, 2014 and Consumer Product Safety Commission (CPSC) posted the press release on 02/20/2014. CPSC posted the press release on the CPSC website. The CPSC recall press release dated February 20, 2014 informed consumers should stop using this product unless otherwise instructed and it is illegal to resell or attempt to resell a recalled consumer product. The CPSC press release contains a Recall Summary with the name of product, hazard, remedy, consumer contact information "Infantino toll-free at (888) 808-3111 between 8 a.m. and 4 p.m. PT Monday through Friday or online at www.infantino.com and click on Recall Information on the home page.", Recall Details on the number of units, description, incidents/injuries, remedy, sold exclusively at Target stores nationwide, Importer, Manufactured in China, and CPSC Consumer Information Hotline and Media Contact. The CPSC press release also contained photos of the product. Infantino, LLC also posted on their company website information on this recall.
Quantity in commerce: 144,000 units
Distribution: US nationwide.
Product codes and lots: Model # 206-647. All lot numbers are included in the scope of the recall

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1313-2014
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1313-2014	Class II	Terminated	Voluntary: Firm initiated	2014-04-09	2014-04-01

Product code MEF

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)