FDA recall record

Reese Pharmaceutical Company Orange Flavor Immune Support Dietary Supplement Effervescent recall — FDA F-0409-2018

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

Class IIclassification
F-0409-2018official record ID
Dec 6, 2017report date

Recall record at a glance

Official recordF-0409-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmReese Pharmaceutical Company
Report dateDec 6, 2017
Recall initiation dateAug 31, 2017
Quantity610,840 units/10 tablets
LocationCleveland, OH, United States

Official 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.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.