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Lower risk Food recall · FDA · Published March 19, 2019

Walgreens Probiotic Recall: Incorrect Strain Used

Walgreens recalls probiotic supplements because the product contains L. acidophilus La-5 instead of the labeled La-14 strain.

🇺🇸 FDA recall #F-1275-2019FoodWalgreens ›
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Recalling firmMerical, LLC233 E Bristol Ln · Orange, CA 92865-2715
✎ GovInfoNow plain-language explainer

Merical, LLC is recalling Walgreens Probiotic 12.5 Billion Active Cultures (30 capsules) because the formulation used the wrong bacterial strain. The product contains L. acidophilus La-5 instead of the L. acidophilus La-14 strain stated on the label. This is a Class III recall involving incorrect labeling of dietary supplement ingredients. Read more at govinfonow.com/recall/17651-walgreens-probiotic-recall-incorrect-strain-used.

Source Summary by GovInfoNow · govinfonow.com/recall/17651-walgreens-probiotic-recall-incorrect-strain-used · Updated October 11, 2026 · FDA enforcement record: FDA #F-1275-2019

Cite this page

“Walgreens Probiotic Recall: Incorrect Strain Used.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/17651-walgreens-probiotic-recall-incorrect-strain-used. Based on FDA recall #F-1275-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1275-2019%22&limit=1).

The FDA announced on March 19, 2019, that Merical, LLC is recalling Walgreens Probiotic 12.5 Billion Active Cultures because the product contains an incorrect probiotic strain. The agency classified the recall as Class III.

How to tell if you have it

  • Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules
  • UPC: 311917191119
  • Item Number: 981914
  • Product Number: WGNS 981914
  • Pkg Numbers: 834627045 and 903727801
  • Expiration Dates: 06/20

The hazard

The probiotic blend contains L. acidophilus La-5 strain instead of the L. acidophilus La-14 strain stated on the label, according to the FDA.

Context

GovInfoNow's records show Merical, LLC has issued three other recalls since October 31, 2019. On January 9, 2020, a Merical glucosamine supplement was recalled for lacking a shellfish allergen warning. Other recent recalls of similar products include Member's Mark Super Greens (October 24, 2025), Wellnov Liposomal D3-5000IU Spray (April 23, 2026), Wellnov Liposomal D3+B12 Spray (April 23, 2026), and Wellnov Liposomal Sleep Spray (April 23, 2026).

How to tell if you have this one

Check for Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules with Item Number 981914 and Product Number WGNS 981914. Look for UPC Code 311917191119. Verify the expiration date is 06/20 and check package numbers 834627045 or 903727801.

  • Brand
    Walgreens
  • Product
    Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's
  • Category
    Food

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “One customer in IL and then to retail stores nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Mar 19, 201912. FDA classified it Class III: Apr 10, 201923. Published in FDA’s Enforcement Report: Apr 17, 201934. FDA terminated the recall: Jan 28, 2020420192020
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1275-2019 (March 19, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1275-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA