Food Recall Check
Class I · High risk Terminated Initiated Mar 29, 2024 (3 years ago)

Sensible Portions brand Garden Veggie Straws Sea Salt recall

Recalled by The Hain Celestial Group INC · Hoboken, NJ, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared milk

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Sensible Portions brand Garden Veggie Straws Sea Salt. 1 oz bag UPC:2951530057 Packaged in a 30 CT Variety Pack that contains Sea Salt, Cheddar Cheese, and Zesty Ranch in plastic bags. (15 sea salt, 10 ranch, 5 cheddar cheese) UPC: 29515-32543

Quantity: 2,592 cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Outer Case: 03SEP24MT, 26AUG24MT, 27AUG24MT, 25AUG24MT, 21AUG24MT Individual 1 oz. Bag: 27AUG24MT

Where it was sold

Arkansas Georgia Massachusetts Mississippi North Carolina New Jersey Ohio Oklahoma Pennsylvania

FDA's distribution note: Distributed to distribution centers and depots in MA, NJ, GA, NC, PA, AR, MS, OH, and OK

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
The Hain Celestial Group INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 29, 2024
In FDA report of
May 22, 2024
Terminated
Nov 13, 2024
FDA recall number
F-1239-2024 · event 94353
Official record
FDA enforcement report search