FDA Food Recalls

Recalls / Class II

Class IIF-1533-2022

Product

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles

Type
Food
Affected lot / code info
Batch Numbers: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Lot Numbers: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Product Number: 80338569, 80365757 Item UPC: 323900041073 Case UPC: 10323900041070 Expiration Dates: 0240C60405 07/31/2022, 0314C60402 10/31/2022, 11664334R2 - 05/31/2023, 11664334R3 - 05/31/2023, 11664334R4 - 05/31/2023, 11664334R5 - 05/31/2023, 11664334E1 - 05/31/2023, 12164334E1 07/31/2023, 12164334E2 - 07/31/2023, 12164334Y1 - 07/31/2023, 12164334Y2 - 07/31/2023, 12164334Y3 - 07/31/2023, 12164334Y4 - 07/31/2023, 12164334Y5 - 07/31/2023, 12164334Y6 - 07/31/2023, 12184334E1 - 07/31/2023, 12184334E2 - 07/31/2023, 12184334E3 - 07/31/2023, 12184334E4 - 07/31/2023, 12184334Y1 - 07/31/2023, 12184334Y2 - 07/31/2023, 12184334Y3 - 07/31/2023, 12184334Y4 - 07/31/2023, 12374334D1 - 07/31/2023, 12374334D2 - 07/31/2023, 12374334E0 - 07/31/2023, 12374334E1 - 07/31/2023, 12374334E2 - 07/31/2023, 12374334E3 - 07/31/2023, 12374334E4 - 07/31/2023, 12374334E5 - 07/31/2023, 12374334E6 - 07/31/2023, 12374334E7 - 07/31/2023, 12374334E8 - 07/31/2023, 12374334E9 - 07/31/2023, 12374334EA - 07/31/2023, 12374334Y1 - 07/31/2023, 12374334Y2 - 07/31/2023, 13214334D1 10/31/2023, 13214334D2 - 10/31/2023, 13214334J1 - 10/31/2023, 13214334K0 - 10/31/2023, 13214334K1 - 10/31/2023, 13214334K2 - 10/31/2023, 13214334K3 - 10/31/2023, 13214334K4 - 10/31/2023, 13214334K5 - 10/31/2023, 13214334K6 - 10/31/2023, 13214334K7 - 10/31/2023, 13214334K8 - 10/31/2023, 13214334K9 - 10/31/2023, 13214334P1 - 10/31/2023, 13214334P2 - 10/31/2023, 13624334S1 10/31/2023, 20124334E1 12/31/2023, 20124334E2 - 12/31/2023, 20124334E3 - 12/31/2023, 20124334K1 - 12/31/2023, 20124334K2 - 12/31/2023, 20124334K3 - 12/31/2023, 20124334K4 - 12/31/2023, 20384334E1 01/31/2024, 20384334E2 01/31/2024, 20384334E3 10/31/2024
Quantity
82,433 cases

Why it was recalled

Acidified/Low Acid dietary supplement with no approved process.

Recalling firm

Firm
The Procter & Gamble Company
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
1 Procter And Gamble Plz, N/A, Cincinnati, Ohio 45202-3315

Distribution

Distribution pattern
Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia.

Timeline

Recall initiated
2022-07-12
FDA classified
2022-08-03
Posted by FDA
2022-08-10
Terminated
2024-08-15
Status
Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-1533-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings.