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Recall Number: F-0408-2018

Why was Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the following brand names: Discount Drug Mart UPC 0 93351 01230 3; Good Neighbor Pharmacy UPC 0 87701 41330 8; Hyvee UPC 0 75450 09537 1; Kinray Preferred Plus UPC 0 23513 01010 6; Live Better UPC 0 41310 62998 7; Meijer UPC 7 08820 15073 7; Premier Value UPC 8 40986 02972 1; QC UPC 6 35515 96938 4; Rite Aid UPC 0 11822 95098 5; Shopko UPC 4 00114 22672 1; ShopRite UPC 0 41190 22784 6; Top Care UPC 0 36800 40632 2 & UPC 0 36800 40632 2; Western Family UPC 0 15400 12657 1 & Winco UPC 0 70552 24153 4. recalled?

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

Check out this page for guidance on what to do if you've consumed food from recall F-0408-2018 .

Reese Pharmaceutical Company recall in Cleveland, OH details
Here's recall specific data. Click on the company, city, or state for more recalls by Reese Pharmaceutical Company or more recalls in Cleveland or Ohio.

  • City: Cleveland

  • State: Ohio

  • Country: United States

  • Classification: Class II

  • Classification Date: 2017-11-30

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

  • Product Description: Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the following brand names: Discount Drug Mart UPC 0 93351 01230 3; Good Neighbor Pharmacy UPC 0 87701 41330 8; Hyvee UPC 0 75450 09537 1; Kinray Preferred Plus UPC 0 23513 01010 6; Live Better UPC 0 41310 62998 7; Meijer UPC 7 08820 15073 7; Premier Value UPC 8 40986 02972 1; QC UPC 6 35515 96938 4; Rite Aid UPC 0 11822 95098 5; Shopko UPC 4 00114 22672 1; ShopRite UPC 0 41190 22784 6; Top Care UPC 0 36800 40632 2 & UPC 0 36800 40632 2; Western Family UPC 0 15400 12657 1 & Winco UPC 0 70552 24153 4.

  • Report Date: 2017-12-06

  • Product Type: Food

  • Company: Reese Pharmaceutical Company

  • Status: Terminated

  • Recall Number: F-0408-2018

  • Postal Code: 44106-4218

  • Recall Initiation Date: 2017-08-31

  • Recall End Date: 2018-06-04

  • Event ID: 78192

  • 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.

  • Voluntary Or Mandated: Voluntary: Firm initiated

  • Initial Firm Notification: Letter

  • Extra Info: All lots

  • Product Quantity: 287,856 units/10 tablets

  • Address: 10617 Frank Ave

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