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High RiskFDAfda-F-0784-2016UNDECLARED ALLERGEN

Dried lactose powder, product sold under brand Wine-King Beer-King, packaged in three consumer-sized plastic bags of 4 oz., 1 Lb. and 5 ...

Category
Units Affected
55
Recall Date
February 25, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0784-2016.

Dried Lactose powder product, which is used in brewery to make beer, does not declare whey or milk and the label declared lactose only.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0784-2016.

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 Northwest Specialty, 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-0784-2016.

Northwest Specialty, Inc.

FDA

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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.

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Northwest Specialty, Inc. Recall FAQ

Northwest Specialty, Inc. is the subject of a food safety report: Dried lactose powder, product sold under brand Wine-King Beer-King, packaged in three consumer-sized plastic bags of 4 oz., 1 Lb. and 5 .... The notice was published on February 25, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 55 units are potentially affected.