Frozen baby bhindi recalled after testing positive for Salmonella
Chetak New York is recalling Deep-brand frozen baby bhindi 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 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: Open seals in the packaging which may compromise the sterility of the product. The notice does not report any illnesses, injuries or deaths. The notice states: "may exhibit open seals in the packaging which may compromise the sterility of the product"
Plain-English summary
Deep-brand Premium Select Baby Bhindi, 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 24536, 25007, 25035, 25053, 25078, 25081, 25132, 25163, 25193. 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 baby bhindi 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
- Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS
- Manufacturer
- Medline Industries, LP
- Category
- Food — Frozen produce
- Affected units
- 1,566,500
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 (4)
- UDI/DI 30888277715947 (each)
- 10888277715943 (box)
- 20888277715940 (case)
- ALL LOTS
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 7 recalled by Medline Industries, LP 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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