Skip to main content
High RiskFDAfda-F-1314-2013OTHER

Canned Apricot in Light Syrup or canned Apricot in Heavy Syrup. The PDP reads "HOOD-CREST APRICOTS UNPEELED HALVES IN LIGHT SYRUP NET ...

Category
Units Affected
0
Recall Date
February 8, 2013
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1314-2013.

Potentially under processed and reports of swollen and bursting cans as well as fruit browning quickly after opening the can and undercooked (firm) fruit from consumers.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1314-2013.

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 Sage Creek 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-1314-2013.

Sage Creek 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

Sage Creek Inc Recall FAQ

Sage Creek Inc is the subject of a beverages safety report: Canned Apricot in Light Syrup or canned Apricot in Heavy Syrup. The PDP reads "HOOD-CREST APRICOTS UNPEELED HALVES IN LIGHT SYRUP NET .... The notice was published on February 8, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.