Scalpa Numb Maximum Strength Topical Anesthetic Cream
Summary
CPSC recall: Scalpa Numb Maximum Strength Topical Anesthetic Cream. By Scalpa Inc., of Phoenix, Ariz.. Hazard: The product contains the substance lidocaine which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning to young children.. Remedy: Consumers should immediately stop using the recalled Scalpa Numb, store the cream in a safe location out of reach of children and cont
Details
Source
CPSC Consumer Product Recall
External ID
8988
Action Date
2021-01-14
Status
Recalled
Category
consumer_product
Product Description
This recall involves Scalpa Numb Maxium Strength Topical Anesthestic Cream in a 10 gram black and white tube with a whit
Context & Analysis
This is a unclassified recall.
This was one of 6 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Scalpa Inc., of Phoenix, Ariz. has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Scalpa Inc., of Phoenix, Ariz.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Scalpa Inc., of Phoenix, Ariz. have FDA actions?
Scalpa Inc., of Phoenix, Ariz. has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "8988" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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