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Class II: temporary or reversible health riskTerminated

Reese Pharmaceutical Orange Flavor Immune Support Dietary Recall

Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle

Reese Pharmaceutical Company · Cleveland, OH

Risk level
Class II
Reported by FDA
Dec 6, 2017
Recall ID
F-0409-2018
Check your lot numberHow we source this data

Summary

Reese Pharmaceutical recalled Orange Flavor Immune Support Dietary starting Aug 31, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0409-2018 on Dec 6, 2017. Reason: The label does not list "Sodium" in the ingredient statement. Status: Terminated.

Why it was recalled

The label does not list "Sodium" in the ingredient statement.

Product description

Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the following brand names: Best Choice UPC 0 70038 60863 9 & UPC 0 70038 60863 9; Discount Drug Mart UPC 0 93351 00909 9; Freds Mart UPC 0 84579 12451 0; Good Neighbor Pharmacy UPC 0 87701 40672 0; Health Accents UPC 7 25439 95738 0; Health Mart UPC 0 52569 14073 4; Hyvee UPC 0 75450 06187 1; Kinray Preferred Plus UPC 0 23513 81512 1; Leader UPC 0 96295 13167 3 & UPC 0 96295 12239 8; Live Better UPC 0 41310 62997 0; Meijer UPC 7 08820 15072 0; Premier Value UPC 8 40986 01982 1; QC UPC 6 35515 95513 4; Reese UPC 0 23513 81512 1; Rite Aid UPC 0 11822 45092 8; Select Brand UPC 0 15127 02433 4; Shopko UPC 4 00125 10186 4; ShopRite UPC 0 41190 22785 3; Top Care UPC 0 36800 38123 0 & UPC 0 36800 38123 0; Western Family UPC 0 15400 12656 4 & Winco UPC 0 70552 24154 1.

Lot numbers, UPCs & expiration codes

All lots

Where it was sold

Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV & WY.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0409-2018
Classification
Class II
Status
Terminated
Recall initiated
Aug 31, 2017
FDA report date
Dec 6, 2017
Quantity
610,840 units/10 tablets
Recall type
Voluntary: Firm initiated
Recalling firm
Reese Pharmaceutical Company

Original FDA data

Every field from FDA enforcement report F-0409-2018, exactly as published.

Show all FDA fields
City
Cleveland
State
OH
Status
Terminated
Country
United States
Event ID
78192
Address
10617 Frank Ave
Code information
All lots
Postal code
44106-4218
Report date
Dec 6, 2017
Product type
Food
Recall number
F-0409-2018
Classification
Class II
Recalling firm
Reese Pharmaceutical Company
Product quantity
610,840 units/10 tablets
Termination date
Jun 4, 2018
Reason for recall
The label does not list "Sodium" in the ingredient statement.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the following brand names: Best Choice UPC 0 70038 60863 9 & UPC 0 70038 60863 9; Discount Drug Mart UPC 0 93351 00909 9; Freds Mart UPC 0 84579 12451 0; Good Neighbor Pharmacy UPC 0 87701 40672 0; Health Accents UPC 7 25439 95738 0; Health Mart UPC 0 52569 14073 4; Hyvee UPC 0 75450 06187 1; Kinray Preferred Plus UPC 0 23513 81512 1; Leader UPC 0 96295 13167 3 & UPC 0 96295 12239 8; Live Better UPC 0 41310 62997 0; Meijer UPC 7 08820 15072 0; Premier Value UPC 8 40986 01982 1; QC UPC 6 35515 95513 4; Reese UPC 0 23513 81512 1; Rite Aid UPC 0 11822 45092 8; Select Brand UPC 0 15127 02433 4; Shopko UPC 4 00125 10186 4; ShopRite UPC 0 41190 22785 3; Top Care UPC 0 36800 38123 0 & UPC 0 36800 38123 0; Western Family UPC 0 15400 12656 4 & Winco UPC 0 70552 24154 1.
Distribution pattern
Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV & WY.
Recall initiation date
Aug 31, 2017
Initial firm notification
Letter
Center classification date
Nov 30, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0409-2018, published Dec 6, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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