FDA recall record

Reese Pharmaceutical Company Berry Flavor Immune Support Dietary Supplement Effervescent recall — FDA F-0408-2018

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

Class IIclassification
F-0408-2018official record ID
Dec 6, 2017report date

Recall record at a glance

Official recordF-0408-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmReese Pharmaceutical Company
Report dateDec 6, 2017
Recall initiation dateAug 31, 2017
Quantity287,856 units/10 tablets
LocationCleveland, OH, United States

Official 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.

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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