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Lower risk Food recall · FDA · Published July 30, 2018

Driscoll's Strawberries Recall: Potential Blood Contamination Risk

Driscoll's recalls 16oz strawberries due to potential blood contamination. Consumers should check for the specific lot code and contact Driscoll's for details.

🇺🇸 FDA recall #F-1838-2018FoodDriscoll's ›
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Contact the company

Recalling firmDriscoll's Strawberry Associates, Inc.345 Westridge Dr · Watsonville, CA 95076-4169
✎ GovInfoNow plain-language explainer

What happened, in plain English

Driscoll's is recalling 16-ounce strawberries that may contain blood. This could pose a risk of foodborne illness if consumed. The recall affects products sold in the USA with specific lot codes. Read more at govinfonow.com/recall/18792-driscoll-s-strawberries-recall-potential-blood-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/18792-driscoll-s-strawberries-recall-potential-blood-contamination-risk · Updated October 6, 2026 · FDA enforcement record: FDA #F-1838-2018

Cite this page

“Driscoll's Strawberries Recall: Potential Blood Contamination Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18792-driscoll-s-strawberries-recall-potential-blood-contamination-risk. Based on FDA recall #F-1838-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1838-2018%22&limit=1).

Why it’s dangerous

Blood contamination in strawberries could lead to foodborne illness if the contaminated berries are eaten. This is a potential risk due to the handling process during harvest or packing.

Who’s affected

Consumers who purchased Driscoll's 16-ounce strawberries in the USA are affected. Those with allergies to blood products or food safety concerns are at slightly higher risk.

How to tell if you have this one

Check for the lot code on the packaging, which includes the code 003 11284 0728. The product was sold in the USA and comes from Watsonville, California.

  • Brand
    Driscoll's
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot code 003 11284 0728 on the packaging to identify affected items.

Where it went and when

Where it was distributed

Distributed in Arizona and California, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “AZ, CA and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California.

Recall timeline

FDA terminated this recall 22 days after the firm started it.

1. Firm started the recall: Jul 30, 201812. FDA classified it Class II: Aug 21, 201823. FDA terminated the recall: Aug 21, 201834. Published in FDA’s Enforcement Report: Aug 29, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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

✎ GovInfoNow

Questions people ask

What should I do if I have the affected product?

The recall does not include a specific remedy, so contact Driscoll's directly for further instructions.

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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-1838-2018 (July 30, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1838-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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