art monkey llc dba why not naturalfoodHigh PriorityExpired

Art Monkey Llc Dba Why Not Nat Why Not Natura Recall (Sal...

Why Not Natural Moringa Capsules lot A25G051 were recalled because of potential Salmonella contamination. FDA openFDA now lists recall H-0510-2026 as Terminated as of April 3, 2026; keep the details for historical verification.

By RecallRadar Editorial Team

Sourced from FDA. Last verified March 4, 2026.

On this page

Free checker

Check if you qualify

See whether your device may qualify for a free repair or replacement program before you spend money.

Check if you qualify

Key facts

Date announced
January 28, 2026
Source agency
FDA

This recall involves safety concerns. Take action promptly.

Plain-English Summary

Why Not Natural Moringa Capsules lot A25G051 were recalled because of potential Salmonella contamination. FDA openFDA now lists recall H-0510-2026 as Terminated as of April 3, 2026; keep the details for historical verification.

Is This Recall Still Active?

Status: No - Expired

This recall is no longer active. You can still review details here for historical reference and confirmation.

What's Being Recalled

Quoted source excerpt from the official notice.

Potential to be contaminated with Salmonella

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand
Art monkey llc dba why not natural
Category
food
Source agency
FDA
Announced
January 28, 2026
Expires
April 3, 2026
Country
US
Status
Expired

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

lot # A25G051

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

  1. 1## Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom. Agency: FDA | Category: food | Date: 2026-01-28 Reason: Potential to be contaminated with Salmonella What to do:
  2. 2Stop using the product if it matches your lot/model.
  3. 3Compare your product details with the FDA recall notice.
  4. 4Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

This program has ended. The official source page may no longer be available.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source
FDA
Announced by source
January 28, 2026
Last reviewed by RecallRadar
March 4, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists lot # A25G051.

What is the remedy for this recall?

## Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom. Agency: FDA | Category: food | Date: 2026-01-28 Reason: Potential to be contaminated with Salmonella What to do: 1. Stop using the product if it matches your lot/model. 2. Compare your product details with the FDA recall notice. 3. Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/food/enforcement.json?search=recall_number.exact:%22H-0510-2026%22&limit=1

Keep browsing with these internal hubs: art monkey llc dba why not natural recall hub and Food & Drug recall hub.

Official Resources

Use these primary sources for final eligibility and claim instructions.

View official notice from FDA

See an inaccuracy?

Help us improve the accuracy of this recall information.

500 characters remaining

Related Recalls

Clobetasol propionate
High PriorityActive

Clobetasol Propionate Cream USP, 0.05%, 60 g tube, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, United States, Manufactured by: Lupin Limited, Pithampur (MP) 454 775, INDIA, NDC 68180-956-04.

Failed content uniformity specifications.

Sep 2, 2026

Levothyroxine sodium
High PriorityActive

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-453-17.

Subpotent Drug

Sep 2, 2026

Acthar
High PriorityActive

Acthar Gel (repository corticotropin injection), 5 mL multiple-dose vial, Rx Only, Mfd. for: Mallinckrodt ARD LLC, Bridgewater, NJ 08807, NDC 63004-8710-1 & NDC 63004-8710-2

Presence of particulate matter: glass and stopper piece

Sep 2, 2026

Levothyroxine sodium
High PriorityActive

Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-448-17.

Subpotent Drug

Sep 2, 2026

Tyenne
High PriorityActive

Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, Illinois, 60047, NDC 65219-594-20.

Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.

Sep 2, 2026