Biotouch Inc., of City of Industry, Calif. recalls
1 recall recorded since 2018, most recently on 28 February 2019. Status and classification are as published by the CPSC.
Recalls1
Ongoing (FDA)0
Terminated or completed0
Class I (FDA)0
Announced Consumer products
- Recall started
- 28 February 2019
- Reason
- The package is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving gel contains lidocaine, posing a risk of poisoning to young children.
- Remedy
- Consumers should immediately place the recalled topical anesthetic out of reach of children and contact Biotouch for instructions on how to obtain a full refund, including shipping.
- Recall number
- 19075
- EZY Gel Topical Anesthetic Gel
CPSC recall notice
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.