CLASS II Food recall · Reported 17 Nov 2021 · FDA Enforcement Report

Instant Pure-flo F bag) food grade starch material 12151103CA recalled

Ingredion is recalling Instant Pure-flo F bag) food grade starch material 12151103CA, distributed in 16 states. The recall was initiated on 29 Oct 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch JA2423 Batch JA2427 Batch JA2431 Batch KA2435 Batch KA2441 Batch KA2445 Batch KA2449 Batch KA2453 Batch KA2459

Quantity recalled21,623 50 lb. bags

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0135-2022
FDA event ID: 88985
Recalling firm: Ingredion, Westchester, IL
Classification: Class II
Status: Terminated
Recall initiated: 29 Oct 2021
FDA classified: 10 Nov 2021
Reported: 17 Nov 2021
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Foreign Material
Product category: Other

Timeline

29 Oct 2021	Recall initiated by company
10 Nov 2021	Classified by FDA	+12 days
17 Nov 2021	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for metal fragments in product

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Ingredion INSTANT PURE-FLO F (50 pound bag) food grade starch material 12151103CA

Where it was distributed

Distributors and manufacturers in: AR, CA, GA, IL, KY, MA, MI, MO, NC, NJ, NY, OH, PA, TX, WA, WI, CANADA, COLUMBIA, MEXICO

Arkansas California Georgia Illinois Kentucky Massachusetts Michigan Missouri North Carolina New Jersey New York Ohio Pennsylvania Texas Washington Wisconsin

Questions about this recall

Why was it recalled?

Potential for metal fragments in product

Which lots are affected?

Batch JA2423 Batch JA2427 Batch JA2431 Batch KA2435 Batch KA2441 Batch KA2445 Batch KA2449 Batch KA2453 Batch KA2459

Where was it sold?

Distributors and manufacturers in: AR, CA, GA, IL, KY, MA, MI, MO, NC, NJ, NY, OH, PA, TX, WA, WI, CANADA, COLUMBIA, MEXICO

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Ingredion

All 5

Reported	Class	Recall	Company	Reason	Where
27 Oct 2021Food	CLASS II	Instant Pure-flow F Food Starch, material 12151103CA recalled	Ingredion	Foreign Material	IN, NJ, OH
15 Sep 2021Food	CLASS II	Fermentation Derived Pepsin Product packaging recalled by IngredionFermentation Derived	Ingredion	Undeclared Egg	10 states
5 Feb 2020Food	CLASS II	Ultra-TEX4 Food Starch recalled by Ingredion Incorporated	Ingredion	Foreign Material	7 states
16 Mar 2016Food	CLASS II	Cornstach packaged in a 50lb. bag with white and green label recalledCornstach	Ingredion	Foreign Material	KS

Other Other recalls

All 4,664

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Food	CLASS I	Alfalfa, Net Weight 50 lbs. bag, Product of USA, International recalledAlfalfa	International Sprout Holdings	Salmonella	17 states
16 Sep 2026Food	CLASS I	Crown Farms Dried Suri Cut, 200 gm per, keep frozen recalledCrown	Euro Foods Group USA NJ	Foreign Material	4 states
9 Sep 2026Food	CLASS I	Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic recalledItem	Ron's Home Style Foods	Salmonella	AR, OK, TX
9 Sep 2026Food	CLASS I	Food to Live Organic SuperGrass Powder recalled by Lexunder	Lexunder	Salmonella	40 states
3 Sep 2026Food	ANNOUNCED	Epinephrine Injection, USP 30 mg/ (1 mg/mL) multi dose vial recalledAmerican Regent, Inc.	American Regent	Particulate Matter	Nationwide