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