Recall Radar

Merical recalls Walgreens Probiotic 12.5 Billion Active Cultures: label issue

April 17, 2019 · Merical Class III

Class IIIFDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.
Reason for the recallIncorrect probiotic strain used in formulation which did not match product labeling.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Merical
Location
Orange, CA
Reported by FDA
April 17, 2019
Recall started
March 19, 2019
Risk class
Class III
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Labeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's L. rhamnosus HN001, L acidophilus La-14, L reuteri L.RE02. Other ingredients: Cellulose, Gelatin, Silicon Dioxide, Magnesium Stearate (vegetable source)/ Item Number: 981914 Product Number: WGNS 981914 UPC Code: 311917191119 product contains L. acidophilus La-5 strain instead of L. acidophilus La-14 strain as stated on the label. Distributed by Walgreen Co, Deerfield, IL
    Quantity: 323 Packaged Cases
    Codes: Pkg Numbers: 834627045 and 903727801; Expiration Dates: 06/20

Where it was distributed

One customer in IL and then to retail stores nationwide.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Merical recalled 1 product, including Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's L. rhamnosus HN001….

Why was it recalled?

Incorrect probiotic strain used in formulation which did not match product labeling.

What does Class III mean?

FDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.

Where was it sold or shipped?

One customer in IL and then to retail stores nationwide.

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

More recalls from Merical

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Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.