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Stop using now Food recall · FDA · Published December 4, 2025

Member's Mark Jumbo Raw Shrimp Recalled for Chloramphenicol

AZ Gems recalls Member's Mark Jumbo Raw Shrimp due to elevated chloramphenicol levels. Check UPCs and best-by dates.

🇺🇸 FDA recall #H-0401-2026FoodMember's Mark ›
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Recalling firmAZ Gems, Inc.405 Missouri Ct · Redlands, CA 92373-8083
✎ GovInfoNow plain-language explainer

What happened, in plain English

AZ Gems, Inc. is recalling Member's Mark branded Jumbo Raw Shrimp because the product contains elevated levels of chloramphenicol, an antibiotic that is prohibited in food animals in the United States. The recall covers approximately 1,099 cases distributed nationwide under the Member's Mark label. Consumers should check their freezers for specific lot codes and expiration dates to determine if they possess a recalled item. Read more at govinfonow.com/recall/6919-member-s-mark-jumbo-raw-shrimp-recalled-for-chloramphenicol.

Source Summary by GovInfoNow · govinfonow.com/recall/6919-member-s-mark-jumbo-raw-shrimp-recalled-for-chloramphenicol · Updated October 9, 2026 · Official notice: FDA #H-0401-2026

Cite this page

“Member's Mark Jumbo Raw Shrimp Recalled for Chloramphenicol.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6919-member-s-mark-jumbo-raw-shrimp-recalled-for-chloramphenicol. Based on FDA recall #H-0401-2026.

Why it’s dangerous

Chloramphenicol is a prescription antibiotic that is banned for use in food-producing animals in the U.S. due to potential serious health risks, including bone marrow suppression and aplastic anemia, even in small amounts. Consuming shrimp with elevated levels poses an unnecessary health risk.

Who’s affected

Consumers who purchased frozen shrimp from retailers carrying the Member's Mark brand, likely Sam's Club or similar warehouse clubs. Individuals who have not yet cooked or consumed the product are at risk of ingesting prohibited antibiotic residues.

How to tell if you have this one

Look for Jumbo Raw Shrimp packaged under the Member's Mark label. Check the UPC code: 1 93968 00697 6. Verify the Product Codes are 231874 4D20 or 231874 4D21, with Best By dates of 4/19/2026 or 4/20/2026.

  • Brand
    Member's Mark
  • Product
    Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the shrimp if it matches the recalled UPC, product codes, and best-by dates.

  2. Discard or return the item

    The recall record does not specify a specific remedy such as a refund or return process; consumers should contact the retailer where it was purchased for further instructions.

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: “Product was shipped nationwide and distributed exclusively under the Member's Mark label.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 48 days after the firm started it.

1. Firm started the recall: Dec 4, 202512. FDA classified it Class II: Jan 14, 202623. Published in FDA’s Enforcement Report: Jan 21, 2026320252026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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 #H-0401-2026 (December 4, 2025)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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