43%

Fewer recalls than
Supplements & Specialty peers

MeriCal — FDA Recall History & Enforcement Records

Established Player · Supplements & Specialty

Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.

As of July 16, 2026, MeriCal has 5 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 24 Oct 2025. MeriCal is categorized under Supplements & Specialty based on their predominant recall history.

5
Total FDA recalls
7.3
Years in FDA database
0.7
Recalls per year
265 days(0.7 yrs)
Since last recall
20.0%
Class I (life-threatening)
0.7 recalls/yr vs Supplements & Specialty avg 2.3/yrWell Below Average

Recall activity over time for MeriCal

How serious are MeriCal recalls?

FDA recall classifications by severity

Class I (Life-threatening)
20.0% (1 recalls)
Class II (Moderate risk)
40.0% (2 recalls)
Class III (Minor violation)
40.0% (2 recalls)

Full FDA recall history for MeriCal

All 5 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first

Date Product Reason Class & Status
24 Oct 2025Official FDA Notice Member’s Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775 Potential contamination of Salmonella Richmond Class IOngoing
9 Jan 2020Official FDA Notice Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg; Helps Overall Joint Physical Function; Product label does not contain Crustacean Shellfish on the ingredient list or allergen information Class IITerminated
9 Jan 2020Official FDA Notice Meijer Joint Health Movement Advanced Dietary Supplement with Glucosamine + Chondroitin. 1500 mg; Supports Joint Mobil Product label does not contain Crustacean Shellfish on the ingredient list or allergen information Class IITerminated
31 Oct 2019Official FDA Notice Leader Advanced Probiotic with 6 Probiotic Strains and 20 billion Live Cultures. 30 capsules Item Number: CARD40359, P Incorrect Probiotic blend indicated in the Supplemental Facts Panel on product label. Class IIITerminated
19 Mar 2019Official FDA Notice Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU’ Incorrect probiotic strain used in formulation which did not match product labeling. Class IIITerminated

Where have MeriCal recalls occurred?

States affected across all recorded FDA enforcement actions

Nationwide

Where does this recall data come from?

Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.

Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.

To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.

© 2026 FoodRecallFinder.com | Turnkey Trading Unlimited LLC. All rights reserved. FDA recall data sourced from openFDA.gov.

How we calculate these metrics →