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FoodRecallWatch
Class II, May Cause HarmF-0041-2017

Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)

Recalled by Schafer Fisheries on Aug 22, 2013

Reviewed by FoodRecallWatch Editorial Team · Updated

Recall Summary

Schafer Fisheries recalled Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G) in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Aug 22, 2013.

The FDA-published reason for this recall is: "Lack of adequate HACCP records."

The product reached multiple states, recorded by the FDA as "US: IL, NY, CA." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Fulton, IL. The recall covers 250 cases (12 units per case) of product. The FDA has Terminated this recall (first reported Oct 19, 2016), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.

Reason for Recall

Lack of adequate HACCP records.

Product Description

Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)

Distribution

US: IL, NY, CA

What Should You Do?

  • 1.Check your kitchen for this product immediately.
  • 2.Do not consume the recalled product.
  • 3.Return the product to where you bought it for a full refund, or throw it away.
  • 4.If you have experienced any health issues, contact your healthcare provider.

Browse Related Recalls

States affected: California, Illinois, New York

Terms Explained

Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.