TriDerma Recalls Pain Relief Cream for Child-Resistant Packaging Failure
TriDerma is recalling Pain Relief Cream with Lidocaine because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk to young children.
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (poisoning via lidocaine ingestion) where injury has not yet been reported, which aligns with the 'High' severity criteria in the rubric.
Plain-English summary
TriDerma, of Corona, Calif., is recalling approximately 410 units of Pain Relief Cream with 4% Lidocaine. The recall involves the product in a 4-ounce jar and a 2.2-ounce tube. The affected products were sold online at www.triderma.com from January 2018 through April 2019 for approximately $22 for the jar and $15 for the tube.
The recall is due to the packaging's failure to meet the child-resistant closure requirements of the Poison Prevention Packaging Act. Because the cream contains lidocaine, it poses a risk of poisoning to young children if they apply it to their skin or ingest it. No injuries have been reported.
Consumers should immediately store the topical anesthetic in a safe location out of reach of children. They should contact TriDerma at 800-279-7282, email [email protected], or visit www.triderma.com to request a free replacement child-resistant cap. TriDerma is also contacting all known purchasers directly.
The recalled product
- Product
- Pain Relief Cream with Lidocaine
- Manufacturer
- TriDerma, of Corona, Calif.
- Hazard
- Affected units
- 410
Distribution
Distributed nationwide across the United States.
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