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.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: Scored 5 because the FDA has classified this action as Class I, which the rubric maps directly to Critical.
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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