Skip to main content
High RiskFDAfda-F-2088-2016CONTAMINATION

Prime CAP Sugar, S 95-135, Encapsulated Sugar. Ingredients: Sugar and Hydrogenated Palm Oil, #10040870, Net WT. 125 lbs. Poly lined car...

Category
Units Affected
196,000
Recall Date
July 13, 2016
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2088-2016.

Specific lots of Prime Cap Sugar 95-135 is being recalled because of possible contamination caused by metal shavings.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2088-2016.

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 Innovative Food Processors, 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-2088-2016.

Innovative Food Processors, 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

Innovative Food Processors, Inc. Recall FAQ

Innovative Food Processors, Inc. is the subject of a food safety report: Prime CAP Sugar, S 95-135, Encapsulated Sugar. Ingredients: Sugar and Hydrogenated Palm Oil, #10040870, Net WT. 125 lbs. Poly lined car.... The notice was published on July 13, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 196,000 units are potentially affected.