Deep-brand Select Tindora Net Wt. 1 LB 8 oz. (24 oz.) (680 g) KEEP FROZEN
Recalling firm: CHETAK NEW YORK LLC
Why it was recalled
Product tested positive Salmonella .
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 12, 2026.
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Compare the exact product and package details with the label you have.
ProductDeep-brand Select Tindora Net Wt. 1 LB 8 oz. (24 oz.) (680 g) KEEP FROZEN
Package size1 LB
FDA code information
Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
Deep-brand Select Tindora Net Wt. 1 LB 8 oz. (24 oz.) (680 g) KEEP FROZEN
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | 24353 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 24360 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25011 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25031 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25056 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25094 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25099 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25120 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25134 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25149 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
| lot | 25172 | Lot: 24353, 24360, 25011, 25031, 25056, 25094, 25099, 25120, 25134, 25149, 25172 |
Original FDA recall reason
Product tested positive Salmonella .
Recall details
- Recall number
- H-0271-2026
- Event ID
- 97631
- FDA status
- Terminated
- Initiated
- Sep 5, 2025
- Reported
- Dec 17, 2025
- Classified
- Dec 11, 2025
- Terminated
- Feb 12, 2026
- Quantity
- 3509532 bags
- Location
- Union, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
United States
FDA source record · H-0271-2026
Data updated September 16, 2026. View official FDA data ↗
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