RecallHawk

Unity Teeter Tunnels with Lexan Tops

Playworld Systems Inc., of Lewisburg, Pennsylvania

Summary

CPSC recall: Unity Teeter Tunnels with Lexan Tops. By Playworld Systems Inc., of Lewisburg, Pennsylvania. Hazard: If a child accidentally falls underneath the Unity Teeter Tunnel, the end of the seesaw plank can land on them, posing a risk of serious injury and a crush hazard.. Remedy: Consumers should immediately stop using the recalled teeter tunnels and contact Playworld Systems to schedule a free repair. Playworld Systems will send a certified playground installer to each location to repair

Details

Source

CPSC Consumer Product Recall

External ID

10285

Action Date

2025-05-29

Status

Recalled

Category

consumer_product

Product Description

This recall involves Playworld Unity Teeter Tunnels with part numbers ZZXX0182, ZZXX0182S, ZZXX0192 and ZZXX0192S. The s

Context & Analysis

This is a unclassified recall.

This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Playworld Systems Inc., of Lewisburg, Pennsylvania has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Playworld Systems Inc., of Lewisburg, Pennsylvania) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Playworld Systems Inc., of Lewisburg, Pennsylvania have FDA actions?

Playworld Systems Inc., of Lewisburg, Pennsylvania has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10285" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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