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Lower risk Food recall · FDA · Published February 17, 2017

Diamond Crystal Natural Cocoa Powder Recall: Metal Pieces Found in Product

Diamond Crystal recalls Natural Cocoa Powder 10-12% cocoa butter (5 lbs) with metal pieces found during sanitation. Consumers should check UPCs and lot numbers for affected batches.

🇺🇸 FDA recall #F-1626-2017FoodDiamond Crystal ›
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Recalling firmDiamond Crystal Brands Inc100 Center Ave NW · Mitchellville, IA 50169-7709
✎ GovInfoNow plain-language explainer

What happened, in plain English

Diamond Crystal is recalling Natural Cocoa Powder 10-12% cocoa butter (5 lbs) because metal pieces were found missing from the sifter screen during sanitation. This could cause injury if metal fragments are ingested. Read more at govinfonow.com/recall/22203-diamond-crystal-natural-cocoa-powder-recall-metal-pieces-found-in.

Source Summary by GovInfoNow · govinfonow.com/recall/22203-diamond-crystal-natural-cocoa-powder-recall-metal-pieces-found-in · Updated October 8, 2026 · FDA enforcement record: FDA #F-1626-2017

Cite this page

“Diamond Crystal Natural Cocoa Powder Recall: Metal Pieces Found in Product.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22203-diamond-crystal-natural-cocoa-powder-recall-metal-pieces-found-in. Based on FDA recall #F-1626-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1626-2017%22&limit=1).

Why it’s dangerous

During sanitation, metal pieces were discovered missing from the sifter screen. This could lead to metal fragments being present in the cocoa powder, which might cause injury if ingested.

Who’s affected

Anyone who purchased Natural Cocoa Powder 10-12% cocoa butter (5 lbs) with brand names Monarch, Chef's Companion, or other listed brands. People using the product for baking or cooking are most at risk if metal fragments are ingested.

How to tell if you have this one

Check the UPC codes: 50758108102533, 50719098582293, or 10719098582233. Look for lot numbers 024HBA, 025HBA, 026HBA, 027HBA, 028HBA, or 039HBA, 040HBA.

  • Brand
    Diamond Crystal
  • Product
    Natural Cocoa Powder 10-12% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand names: Monarch
  • Category
    Food
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Product distributed to foodservice customers nationwide. There was no foreign/military/government distribution reported.
Recall numberProduct, codes & lotsQuantity
F-1625-2017Baking Powder Net Wt. 5 lbs. (2.27 kg) packaged 6 bags per case, under the following brand names: Chef's Companion UPC 50719098580015, Diamond Crystal Brands, Inc. Savannah, GA 31405; and Sysco UPC 10074865238813, distributed by Sysco Corporation, Houston, TX 77077-2099.; UPC 50719098580015: Lot numbers 023HBA, 024HBA; and UPC 10074865238813: Lot numbers 017HBA, 018HBA, 019HBA, 020HBA, 021HBA, 023HBA1033 cases
F-1626-2017Natural Cocoa Powder 10-12% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand names: Monarch distributed by U.S. Foodservice UPC 50758108102533; Chef's Companion: 1 bag /case, UPC 10719098582233; and 6 bags/case, UPC 50719098582293 Diamond Crystal Brands, Inc. Savannah, GA 31405; UPC 50758108102533: Lot numbers 024HBA, 025HBA, 040HBA; UPC 50719098582293: Lot numbers 024HBA, 025HBA, 026HBA, 028HBA; and UPC 10719098582233: Lot numbers 026HBA, 027HBA, 039HBA, 040HBA.652 cases
F-1627-2017Natural Cocoa Powder 22-24% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand name: Chef's Companion: 1 bag /case, UPC 10719098582240; Diamond Crystal Brands, Inc. Savannah, GA 31405; 026HBA January 26, 2017. 027HBA January 27, 2017. 039HBA Feb. 8, 2017. 040HBA Feb. 9, 2017149 cases
Based on the official FDA remedy

What to do — step by step

  1. Check Product UPC

    Look for the UPC codes listed: 50758108102533, 50719098582293, or 10719098582233.

  2. Identify Lot Numbers

    Check for lot numbers 024HBA, 025HBA, 026HBA, 027HBA, 028HBA, or 039HBA, 040HBA.

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 distributed to foodservice customers nationwide. There was no foreign/military/government distribution reported.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Feb 17, 201712. FDA classified it Class II: Mar 23, 201723. Published in FDA’s Enforcement Report: Mar 29, 201734. FDA terminated the recall: Jun 28, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  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-1626-2017 (February 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1626-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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