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Stop using now Food recall · FDA · Published September 28, 2018

Blackwing Ground Venison Recall: Lead Hazard

Blackwing Meats recalls 10/1lb Ground Venison due to high lead levels. Check your fridge for UPC 7-53390-03000-2.

🇺🇸 FDA recall #F-0061-2019FoodBlackwing Meats ›
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Recalling firmBLACKWING ORGANIC MEATS, INC.19588 W Il Route 173 · Antioch, IL 60002-7220
✎ GovInfoNow plain-language explainer

What happened, in plain English

Blackwing Organic Meats, Inc. is voluntarily recalling its Ground Venison product because it contains high levels of lead. The affected items are packed in a retail box with a cardboard sleeve and roll stock film inside. This recall covers approximately 14 cases or 140 lbs of product distributed in Illinois and Florida. Read more at govinfonow.com/recall/18507-blackwing-ground-venison-recall-lead-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/18507-blackwing-ground-venison-recall-lead-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #F-0061-2019

Cite this page

“Blackwing Ground Venison Recall: Lead Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18507-blackwing-ground-venison-recall-lead-hazard. Based on FDA recall #F-0061-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0061-2019%22&limit=1).

Why it’s dangerous

The product contains high levels of lead, which poses a health risk if ingested. Lead is a toxic metal that can cause serious health issues, particularly in children and pregnant women, though specific symptoms are not detailed in this record.

Who’s affected

Consumers in Illinois and Florida who purchased Blackwing Meats Ground Venison are likely affected. Individuals who consumed the product are at risk due to potential lead exposure.

How to tell if you have this one

Look for Blackwing Meats Ground Venison sold in a retail box containing a cardboard sleeve or roll stock film inside. Check the UPC code for 7-53390-03000-2 and the date code 0308. The product was distributed domestically in Illinois and Florida.

  • Brand
    Blackwing Meats
  • Product
    Blackwing Meats. Inc., Ground Venison, 10/1lb, packed in cardboard sleeve/ roll stock film inside, in aRetail Box
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled Ground Venison due to the risk of lead exposure.

  2. Discard or return the item

    The record does not specify a remedy, so you should dispose of the product or contact the retailer for guidance.

Where it went and when

Where it was distributed

Distributed in Florida and Illinois.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: 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: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew 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: yesFL

FDA distribution: “Domestic: IL, FL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Illinois.

Recall timeline

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

1. Firm started the recall: Sep 28, 201812. FDA classified it Class II: Oct 23, 201823. Published in FDA’s Enforcement Report: Oct 31, 201834. FDA terminated the recall: Feb 7, 2019420182019
  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-0061-2019 (September 28, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0061-2019 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