NuSpice Taco Seasoning
Reason Nu Products Seasoning Product is recalling their F4422 Taco Seasoning may be contaminated with peanut protein due to the ground cumin used in the product.
NuSpice Sazon High Color Seasoning recall
Recalled by Nu Products Seasoning Co. · South Hackensack, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Nu Products Seasoning Product is recalling their F4422 Taco Seasoning and Sazon High Color Seasoning because they may be contaminated with peanut protein due to the ground cumin used in the product.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
NuSpice Sazon High Color Seasoning - F2111, Net Wt: 50 lb, Manufacturer: Nu Products Seasoning Co., 74 Louis Court, South Hackensack, N.J. 07606
Quantity: 250 pounds
Food: Spices & seasonings
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.
Lot #4391 - manufactured on 9/4/14, Lot #'s 4553, 4554, 4555 and 4556 - manufactured on 9/5/14
Where it was sold
New Jersey New York
FDA's distribution note: NJ and NY
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. 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
- Nu Products Seasoning Co.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 9, 2015
- In FDA report of
- Apr 15, 2015
- Terminated
- Jul 13, 2015
- FDA recall number
- F-1917-2015 · event 70283
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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