RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902
Reported: August 4, 2021 Initiated: May 19, 2021 #F-0805-2021
Product Description
RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902
Reason for Recall
Lack of functioning Temperature Indicating Devices in retorts
Details
- Recalling Firm
- Randall Foods, Inc.
- Units Affected
- 800,000 cases (total)
- Distribution
- Retail distribution locations in the following states: Alabama, Arkansas, Florida, Iowa, Illinois, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, North Carolina, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Virginia, Wisconsin, and West Virginia.
- Location
- Tekonsha, MI
Frequently Asked Questions
What product was recalled? ▼
RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902. Recalled by Randall Foods, Inc.. Units affected: 800,000 cases (total).
Why was this product recalled? ▼
Lack of functioning Temperature Indicating Devices in retorts
Which agency issued this recall? ▼
This recall was issued by the FDA Food on August 4, 2021. Severity: Moderate. Recall number: F-0805-2021.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11