Frozen whole surti papdi recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen surti papdi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Wire connected to the electrical box may shift out of its intended position, resulting in electrical arcing. The notice does not report any illnesses, injuries or deaths. The notice states: "Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing."
Plain-English summary
Deep-brand Premium Select Surti Papdi Whole, net weight 12 oz. (340g), labelled KEEP FROZEN, is being recalled by Chetak New York LLC.
The product tested positive for Salmonella.
The recall covers lots 24363, 25011, 25046. 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 papdi 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
- AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps…
- Manufacturer
- Steris Corporation
- Category
- Food — Frozen produce
- Affected units
- 22
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Lot Code: UDI: 00724995176662
- 00724995176679
- 00724995176655 Serial numbers of distributed units: 3619725008
- 3619725011
- 3619725013
- 3621625010
- 3621625011
- 3621625013
- 3621625014
- 3621625015
- 3621925001
- 3621925002
- 3621925005
- 3621925010
- 3622425005
- 3622725005
- 3622725011
- 3622725012
- 3623125006
- 3623425016
Distribution
Part of a larger recall action
This product is one of 2 recalled by Steris Corporation 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.
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