Biotouch Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
U.S. Consumer Product Safety Commission recall (2019-02-28). Hazards: chemical. About 8,500 units in the US.
| Agency | U.S. Consumer Product Safety Commission |
|---|---|
| Recall number | 19075 |
| Published | 2019-02-28 |
| Last updated | 2019-02-28 |
| Products | EZY Gel Topical Anesthetic Gel |
| Firm named in the title | Biotouch |
| Firms | Biotouch Inc., of City of Industry, Calif. (manufacturer); Adventiz Inc. of Chino Hills, Calif. (Online) (distributor) |
| Manufactured in | United States |
| Units (US) | 8,500 |
| Hazard classes | chemical |
| Remedy classes | refund |
| Sold | Biotouch stores, beauty suppliers and tattoo salons nationwide and online at www.amazon.com, www.biotouch.com, www.ebay.com, www.jet.com or www.walmart.com from August 2013 through August 2018 for about $60 |
Description
This recall involves EZY Gel Topical Anesthetic Gel. The recalled product was sold in 1 fluid ounce white bottles. Biotouch Topical Anesthetic Gel EZY Gel is printed on a purple label located on the front panel. Lot numbers and expiration dates are located on the bottom of the bottle.
Hazard
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.
Incidents and injuries
None reported
Machine access
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Source: U.S. Consumer Product Safety Commission recall notice (US Government work). Not affiliated with or endorsed by CPSC. Structured by Data Foundry (product-recall-structuring@2); last changed 2026-09-28. Always confirm with the agency notice.