West des Moines, IA, United States
Hy-Vee Stores Inc recalls
4 recalls recorded since 2018, most recently on 6 May 2024. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls4
Ongoing (FDA)0
Terminated or completed4
Class I (FDA)4
Terminated Class I Food
- Recall started
- 6 May 2024
- Terminated
- 28 June 2024
- Reason
- Potential Salmonella contamination
- Distribution
- IA, IL, KS, MN, MO, NE, SD, WI
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-1304-2024
- Hy-Vee To Go Cookies & Cream Mix, Net wt. 4 oz (113g), UPC 0075450486740, 6 containers per case. Hy-Vee Cookies & Cream Mix, Net Wt. 16oz (453g), UPC 0075450486730, 6 containers per case.
Terminated Class I Food
- Recall started
- 24 May 2021
- Terminated
- 8 July 2021
- Reason
- Product contains chipotle crema as part of a taco kit which contains undeclared major food allergen egg
- Distribution
- Distributed to Hy-Vee grocery stores in IA, IL, KS, MN, MO, NE, SD, WI.
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-0664-2021
- Hy-Vee Chicken Street taco kit, Net Wt. 18 OZ, UPC 282503 212993.
Terminated Class I Food
- Recall started
- 24 November 2020
- Terminated
- 16 December 2020
- Reason
- An ingredient used as an ingredient in the products tested positive for Listeria monocytogenes
- Distribution
- To Hy-Vee stores in IA, IL, KS, MN, MO, NE, SD, and WI.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- F-0174-2021, F-0173-2021
- Hy-Vee, Short Cuts, Pot Roast Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc, West Des Moines, IA UPC 272083 XXXXXX
- Hy-Vee, Short Cuts, Grill Ready Veggie Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc, West Des Moines, IA UPC 272104 XXXXXX
Terminated Class I Food
- Recall started
- 4 January 2019
- Terminated
- 11 February 2019
- Reason
- Product contained an ingredient that tested positive for Salmonella.
- Distribution
- Distributed to consumers in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- F-0826-2019, F-0827-2019, F-0829-2019, F-0832-2019, F-0837-2019, F-0835-2019, F-0825-2019, F-0839-2019, F-0833-2019, F-0834-2019, F-0830-2019, F-0836-2019 and 4 more
- HyVee brand Pumpkin-fluff -flavored cheese cakes packaged in the following ways: 1) Pumpkin-fluff Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 80148 XXXXX packaged in clear plastic containers; 2) Pump
- HyVee brand Smores-flavored Bettercreme cheese cakes packaged in the following ways: 1) Smores Bettercreme Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 82333 XXXXX packaged in clear plastic containers;
- HyVee brand Golden Oreo-flavored cheese cakes packaged in the following ways: 1) Golden Oreo Bettercreme Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 82329 XXXXX packaged in clear plastic containers;
- HyVee brand Pumpkin-flavored Bettercreme cheese cakes packaged in the following ways: 1) Pumpkin Bettercreme Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 82321 XXXXX packaged in clear plastic containers;
- HyVee brand turtle-flavored cheese cakes packaged in the following ways: 1) Turtle Cheesecake, Net Wt. 8 OZ, HyVee West Des Moines, IA UPC 02 82327 XXXXX packaged in clear plastic containers; 2) Turtle Cheesecake,
- HyVee brand Mint chip-flavored Bettercreme cheese cakes packaged in the following ways: 1) Mint Chip Bettercreme Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 82315 XXXXX packaged in clear plastic contain
- HyVee brand Oreo-flavored cheese cakes packaged in the following ways: 1) Oreo Cheesecake, Net Wt. 8 OZ, HyVee West Des Moines, IA UPC 02 80146 XXXXX packaged in clear plastic containers; 2) Oreo Cheesecake Family
- HyVee brand Strawberry-flavored cheese cakes packaged in the following ways: 1) Strawberry Cheesecake, Net Wt. 8 OZ, HyVee West Des Moines, IA UPC 02 80150 XXXXX packaged in clear plastic containers; 2) Strawberry
- and 8 more product lines
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.