CLASS II Device recall · Reported 9 Apr 2014 · FDA Enforcement Report
Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco recalled
Infantino is recalling Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco the Monkey". Non-Fluid Filled, distributed nationwide in the US. The recall was initiated on 6 Jan 2014 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1313-2014
- FDA event ID
- 67582
- Recalling firm
- Infantino, San Diego, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Jan 2014
- FDA classified
- 1 Apr 2014
- Reported
- 9 Apr 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Choking Hazard
- Device type
- Other Medical Devices
Timeline
| 6 Jan 2014 | Recall initiated by company | |
| 1 Apr 2014 | Classified by FDA | +85 days |
| 9 Apr 2014 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco the Monkey". Non-Fluid Filled Teething Ring.
Where it was distributed
US nationwide.
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
Model # 206-647. All lot numbers are included in the scope of the recall
Where was it sold?
US nationwide.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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