Protocol for Life Balance, Phosphatidyl Serine 300mg softgels, 50 count bottle, UPC 707359123922. NOW Foods, Phosphatidy
Summary
The FDA issued a Class III for Protocol for Life Balance, Phosphatidyl Serine 300mg softgels, 50 count bottle, by Now Foods. Reason: Amount of Phosphatidyl Serine in product is less than stated on the label.
Details
Source
Food Recall
External ID
F-0859-2024
Action Date
2024-02-14
Status
Terminated
Category
food
Product Description
Protocol for Life Balance, Phosphatidyl Serine 300mg softgels, 50 count bottle, UPC 707359123922. NOW Foods, Phosphatidyl Serine 300mg softgels, 50 count bottle, UPC 733739023926.
Lot/Code Info: Protocol Lot Number: 3309194 Best By 08/2025 Protocol Lot Number: 3316624 Best By 09/2025 NOW Lot Number: 3309243 Best By 08/2025 NOW Lot Number: 3316650 Best By 09/2025
Quantity Affected: 12,051 bottles
Reason for Recall
Amount of Phosphatidyl Serine in product is less than stated on the label
Distribution
Nationwide and exported to China, Kazakhstan, Czech Republic, Portugal, Kyrgyzstan, Slovakia
Type: Voluntary: Firm initiated
Recall Initiated: 2024-01-10
Company
Bloomingdale, IL
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Now Foods has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class III 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 (Now Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Now Foods have FDA actions?
Now Foods has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0859-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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