Aprepitant capsules and Lidocaine and Prilocaine cream
Sandoz Inc., of Princeton, New Jersey (Lidocaine and Prilocaine cream)
Summary
CPSC recall: Aprepitant capsules and Lidocaine and Prilocaine cream. By Sandoz Inc., of Princeton, New Jersey (Lidocaine and Prilocaine cream). Hazard: The recalled prescription drugs and products that contain lidocaine must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.. Remedy: Consumers should immediately secure the medic
Details
Source
CPSC Consumer Product Recall
External ID
9556
Action Date
2023-03-09
Status
Recalled
Category
consumer_product
Product Description
This recall involves prescription drugs Aprepitant 125 mg capsules sold in cartons containing one blister card of 6 caps
Context & Analysis
This is a unclassified recall.
This was one of 19 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Sandoz Inc., of Princeton, New Jersey (Lidocaine and Prilocaine cream) 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 (Sandoz Inc., of Princeton, New Jersey (Lidocaine and Prilocaine cream)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Sandoz Inc., of Princeton, New Jersey (Lidocaine and Prilocaine cream) have FDA actions?
Sandoz Inc., of Princeton, New Jersey (Lidocaine and Prilocaine cream) 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 "9556" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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