The Recall Desk
Agency classClass IIIOur severity:ModerateFDA (Devices)·Z-0892-2026·Announced 2025-12-17

Frozen surti undhiu mix recalled after testing positive for Salmonella

Chetak New York is recalling Deep-brand frozen surti undhiu mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.

The agency’s classification

FDA (Devices): Class III

Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 2/5 (Moderate).

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: Labeling contains claims that are not consistently present. The notice does not report any illnesses, injuries or deaths. The notice states: "Labeling contains claims that are not consistently present."

Plain-English summary

Deep-brand Premium Select Surti Undhiu Mix, net weight 12 oz. (340 g), labelled KEEP FROZEN, is being recalled by Chetak New York LLC.

The product tested positive for Salmonella.

The recall covers lots IN 25158K, 24358, 25024, 25036, 25052, 25070, 25092, 25098, 25125, 25134, 25158, 25188. The record lists a quantity of 3,509,532 bags for the action, distributed in the United States. The FDA has classified the action as Class I, its most serious category.

Consumers who have surti undhiu mix from these lots should not eat the product and should follow the retailer's return instructions. Anyone who has eaten it and feels unwell should contact a healthcare provider.

The recalled product

Product
Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 7H 38-1008SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 8H; 38-1009SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 9H…
Manufacturer
Orthofix U.S. LLC
Affected units
34,582

Distribution

Distributed nationwide across the United States.

The notice also names 47 states specifically:

Part of a larger recall action

This product is one of 6 recalled by Orthofix U.S. LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →

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