ModerateClass IITerminated

FDA Food recall · Reported December 6, 2017

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; To

Q: Which agency issued this recall?

This recall was issued by the FDA Food on December 6, 2017. Severity: Moderate. Recall number: F-0408-2018.

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: How do I check if my product is affected by a recall?

Check the product description and recall number (F-0408-2018) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.

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-0408-2018
Affected scope: 287,856 units/10 tablets
Initiated: August 31, 2017

Compiled from official public sources by the editorial team. · Updated July 2026

Verify with FDA Food →

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

Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Pr… 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-0408-2018 with the FDA Food before acting.

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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: 288K units
affected scope: Class II
classification: December 6, 2017
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0408-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-0408-2018) was formally reported on December 6, 2017, with the manufacturer initiating the action on August 31, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Reese Pharmaceutical Company is listed as the recalling firm, operating out of Cleveland, OH. Federal records list the affected scope as 287,856 units/10 tablets, a scale large enough to require multi-state distribution tracking.

The documented reason for this recall is: The label does not list "Sodium" in the ingredient statement. Distribution data in the federal record shows the product reached: 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.. Distribution scope 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, 1 from FDA Food - 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 recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.

Severity

Moderate

Affected scope

287,856 units/10 tablets

Related Recalls

1 from same agency

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.

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-0408-2018
Date reported	December 6, 2017
Date initiated	August 31, 2017
Recalling firm	Reese Pharmaceutical Company
Firm location	Cleveland, OH
Affected scope	287,856 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

287,856 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-0408-2018) 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-0408-2018.

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..

How do I check if my product is affected by a recall? ▼

Check the product description and recall number (F-0408-2018) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.

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.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 6, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.