Skip to main content
High RiskFDAfda-F-0061-2019CHEMICAL EXPOSURE

Blackwing Meats. Inc., Ground Venison, 10/1lb, packed in cardboard sleeve/ roll stock film inside, in aRetail Box.

Units Affected
14
Recall Date
September 28, 2018
Issuing Agency
Hazard
Chemical Exposure

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0061-2019.

Blackwing Meats. Inc. is voluntarily recalling Blackwing Venison Ground, 10/1lb. in a Retail Box due to high levels of lead.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0061-2019.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Blackwing Organic Meats, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0061-2019.

BLACKWING ORGANIC MEATS, INC.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Blackwing Organic Meats, Inc. Recall FAQ

Blackwing Organic Meats, Inc. is the subject of a meat & poultry safety report: Blackwing Meats. Inc., Ground Venison, 10/1lb, packed in cardboard sleeve/ roll stock film inside, in aRetail Box.. The notice was published on September 28, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 14 units are potentially affected.