Pain Relief Cream with Lidocaine
Check against the official notice below — it lists the full affected range.
TriDerma has recalled Pain Relief Cream with 4% Lidocaine because the packaging does not meet child-resistant closure requirements under the Poison Prevention Packaging Act. The cream comes in a 4-ounce white jar with a lime green and pink label and white dome cap, or a 2.2-ounce white tube with a lime green and pink label. The recalled products have specific lot numbers ranging from 20189 through 0739A23A, with expiration dates between April 2021 and January 2022, which can be found on the bottom of the jar or the crimped end of the tube.
Since the cream contains lidocaine, young children face a poisoning risk if they apply it to their skin or ingest it. According to the recall, consumers should immediately store the product in a safe location out of reach of children and contact TriDerma for a free replacement child-resistant cap. TriDerma is contacting all known purchasers directly.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
Consumers should immediately store the topical anesthetic in a safe location, out of reach of children and contact TriDerma for a free replacement child-resistant cap. TriDerma is contacting all known purchasers directly.
This recall involves TriDerma Pain Relief Cream with 4% Lidocaine in a jar and tube. The 4 ounce jar is white with a lime green and pink printed label and has a white dome cap. The 2.2 ounce tube is white with a lime green and pink printed label. The lot numbers and expiration dates of the affected products can be found on the bottom of the jar and on the front of the crimped end of the tube. "TriDerma Pain Relief Cream" is printed on the jar and tube. Lot Number Expiration Date 21088 04/2021 20189 04/2021 0738F02A 06/2021 0738F04A 06/2021 0738F04B 06/2021 0738F04C 06/2021 0739A22A 01/2022 0739A22B 01/2022 0739A23A 01/2022
Official record: U.S. Consumer Product Safety Commission ↗
Republished from the official source above; details can change — the source record controls.