CLASS I Food recall · Reported 1 Jun 2023 · USDA FSIS

Frozen, Raw Lamb Products recalled by E.N.A. Meat Packing

E.N.A. Meat Packing is recalling Array. The recall was initiated on 1 Jun 2023 and the FDA has classified it as Class I.

Recall details

Recall number
FSIS-019-2023
Recalling firm
E.N.A. Meat Packing
Classification
Class I
Status
Completed
Recall initiated
1 Jun 2023
Reported
1 Jun 2023
USDA notice type
Closed Recall
Reason category
Processing Deviation
Product category
Other

Timeline

1 Jun 2023Recall initiated by company
1 Jun 2023Published in enforcement report+0 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Array. WASHINGTON, June 1, 2023 – E.N.A. Meat Packing Inc, the importer of record located in Paterson, N.J., is recalling approximately 39,947 pounds of frozen, raw lamb products that were imported without the benefit of import reinspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The frozen, raw lamb items were produced on Feb. 22 through March 13, 2023. The following products are subject to recall [view labels]:  Cartons weighing approximately 40-lb., containing raw frozen pieces of “Simunovic S.A. Frozen Bone in Lamb Leg ABO” produced by Frigorifico Simunovic S.A. with a “Best Before Use By” date of 02/15/2026 to 02/21/2026 and shipping mark ENA036-2023-A. Cartons weighing approximately 47-lb., containing raw frozen pieces of “Frozen Lamb Carcasses” produced by Frigorifico Simunovic S.A. with a “Best Before Use By” date of 02/27/2025 to 03/12/2025 and shipping mark ENA036-2023. The products subject to recall do not bear the USDA mark of inspection. Each carton bears the Chile establishment number 12-01. These items were shipped to a Texas state-inspected facility for further processing. The problem was discovered during routine FSIS monitoring when a shipment of frozen, raw lamb carcasses and bone in lamb leg products imported from Chile was identified that was not presented for FSIS import reinspection. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned

The USDA issues these when meat or poultry was produced without proper inspection, or when a step such as cooking or pasteurisation did not meet requirements.

Product as listed by the USDA

Array

Where it was distributed

Array

Questions about this recall

Why was it recalled?

Array. WASHINGTON, June 1, 2023 – E.N.A. Meat Packing Inc, the importer of record located in Paterson, N.J., is recalling approximately 39,947 pounds of frozen, raw lamb products that were imported without the benefit of import reinspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The frozen, raw lamb items were produced on Feb. 22 through March 13, 2023. The following products are subject to recall [view labels]:  Cartons weighing approximately 40-lb., containing raw frozen pieces of “Simunovic S.A. Frozen Bone in Lamb Leg ABO” produced by Frigorifico Simunovic S.A. with a “Best Before Use By” date of 02/15/2026 to 02/21/2026 and shipping mark ENA036-2023-A. Cartons weighing approximately 47-lb., containing raw frozen pieces of “Frozen Lamb Carcasses” produced by Frigorifico Simunovic S.A. with a “Best Before Use By” date of 02/27/2025 to 03/12/2025 and shipping mark ENA036-2023. The products subject to recall do not bear the USDA mark of inspection. Each carton bears the Chile establishment number 12-01. These items were shipped to a Texas state-inspected facility for further processing. The problem was discovered during routine FSIS monitoring when a shipment of frozen, raw lamb carcasses and bone in lamb leg products imported from Chile was identified that was not presented for FSIS import reinspection. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned

Where was it sold?

Array

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official USDA FSIS notice · Source record retrieved 26 Sep 2026. USDA data is public domain. This page reports the record and gives no medical advice.

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