Recalls / Class II
Class IIF-0785-2023
Product
PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MNCD 800LB TT, PROSANTE TVGPTN 10B MNCD 50LB BG, PROSANTE TVGPTN 10B MNCD 50LB BG 21/P; distributed in bulk tote and paper bags
- Type
- Food
- Affected lot / code info
- 100001356-00223CHXEA 100001356-00323CHXEA 100001356-01023CHXEA 100001356-01123CHXEA 100001356-01223CHXEA 100001356-01323CHXEA 100001356-03223CHXEA 100001356-04523CHXEA 100001356-04623CHXEA 100001356-04723CHXEA 100001356-05823CHXEA 100001356-28422CHXEA 100001356-28522CHXEA 100001356-28622CHXEA 100001356-30722CHXEA 100001356-31822CHXEA 100001356-31922CHXEA 100001356-33422CHXEA 100001356-33522CHXEA 100001356-33622CHXEA 100001356-34922CHXEA 100001361-01123CHXTA 100001361-01223CHXTA 100001361-04423CHXTA 100001364-00323CHXEA 100001364-00423CHXEA 100001364-00523CHXEA 100001364-00623CHXEA 100001364-02523CHXEA 100001364-02623CHXEA 100001364-03323CHXEA 100001364-27822CHXEA 100001364-27922CHXEA 100001364-28122CHXEA 100001364-29822CHXEA 100001364-29922CHXEA 100001364-30022CHXEA 100001364-30122CHXEA 100001364-30822CHXEA 100001364-32222CHXEA 100001364-32422CHXEA 100001364-32522CHXEA 100001364-32622CHXEA 100001364-32722CHXEA 100001364-35522CHXEA 100001364-35622CHXEA 100001364-36122CHXEA 100001364-36222CHXEA 100001364-36322CHXEA 130012781-00323CHXEA 130012781-03223CHXEA 130012781-05123CHXEA 130012781-29722CHXEA 130012781-29822CHXEA 130012781-32522CHXEA
- Quantity
- 4,636,250 lbs
Why it was recalled
Products with a gluten free claim may contain gluten levels above 20 ppm.
Recalling firm
- Firm
- Cargill, Inc Corporate Headquarters
- Notification channel
- Type
- Voluntary: Firm initiated
- Address
- 15407 McGinty Rd W, Wayzata, Minnesota 55391-2365
Distribution
- Distribution pattern
- Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom
Timeline
- Recall initiated
- 2023-03-30
- FDA classified
- 2023-05-01
- Posted by FDA
- 2023-05-10
- Terminated
- 2023-06-08
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0785-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings.