Clinical Resolution Laboratory Topical Anesthetic recall: Failure to Meet Child Resistant Closure
Clinical Resolution Laboratory Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
Why was Clinical Resolution Laboratory Topical Anesthetic recalled?
The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream contains lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.
What should I do if I have this product?
Consumers should immediately place the recalled topical anesthetic out of reach of children and contact Clinical Resolution Laboratory for a full refund, a free replacement cream, or free replacement child-resistant cap. Contact: Clinical Resolution Laboratory toll-free at 877-566-9687 from 8 a.m. to 5 p.m. PT Monday to Friday, email at [email protected] or online at www.clinicalresolution.com and click on the Recall Information tab at the top of the page for more information.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official CPSC record. Only products that match the listed product and identifiers are part of this recall.
- Product
- Numb 100 Topical Anesthetic Cream
- Company
- Clinical Resolution Laboratory, Inc. of Brea, Calif., Laser Jet, Inc. of Brooklyn, N.Y.
- Quantity
- 26500
- Sold at
- Laser Jet and other health and beauty stores nationwide and online at www.amazon.com and www.laserjetinc.com from May 2017 through November 2018 for about $18.
- Recall date
- February 28, 2019
- Incidents / injuries
- None reported
- Agency
- CPSC
Product description
This recall involves Numb 100 Topical Anesthetic Cream. The recalled cream is in a 1.35 fluid ounce white jar with a rounded cap. Numb 100 Topical Anesthetic Cream and a blue cross are printed on the jar's front panel.