ModerateClass IITerminated

FDA Food recall · Reported December 6, 2017

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; Liv

Q: Which agency issued this recall?

This recall was issued by the FDA Food on December 6, 2017. Severity: Moderate. Recall number: F-0409-2018.

Q: Where was the recalled product distributed?

Distribution: 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..

Q: What are the health risks of consuming a recalled food product?

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

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

Recall #: F-0409-2018
Affected scope: 610,840 units/10 tablets
Initiated: August 31, 2017

Compiled from official public sources by the publisher. · Updated September 2026

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Reese Pharmaceutical Company recalled Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. P… - a moderate-severity action.

Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. P… was recalled by Reese Pharmaceutical Company in December 6, 2017. Reason: The label does not list "Sodium" in the ingredient statement.. Check the official notice for the remedy. Verify recall #F-0409-2018 with the FDA Food before acting.

The recall

Reese Pharmaceutical Company issued this moderate-severity FDA Food recall-The label does not list "Sodium" in the ingredient statement..

Moderate
severity level: 611K units
affected scope: Class II
classification: December 6, 2017
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0409-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope (see the Recall Profile below) is large enough to require multi-state distribution tracking. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

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.

Reason for recall

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

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	F-0409-2018
Date reported	December 6, 2017
Date initiated	August 31, 2017
Recalling firm	Reese Pharmaceutical Company
Firm location	Cleveland, OH
Affected scope	610,840 units/10 tablets
Distribution	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.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

610,840 units/10 tablets units affected - multi-state distribution scale.

Regional (<10K units) -

Multi-state (10K – 100K units) -

Large-scale (100K – 1M units) ✓ This recall

Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-0409-2018) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

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

Which agency issued this recall? ▼

This recall was issued by the FDA Food on December 6, 2017. Severity: Moderate. Recall number: F-0409-2018.

Where was the recalled product distributed? ▼

Distribution: 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 are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

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Similar Drugs & Medications · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported December 6, 2017. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026