RecallHawk
Class II Recall

Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sk

Professional Botanicals, Inc.

Summary

The FDA issued a Class II for Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule by Professional Botanicals, Inc.. Reason: Products contains Magnesium Salicylate..

Details

Source

Food Recall

External ID

H-0182-2026

Action Date

2025-11-19

Status

Terminated

Category

food

Product Description

Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.

Lot/Code Info: Lot #: 280914

Quantity Affected: 430 Bottles

Reason for Recall

Products contains Magnesium Salicylate.

Distribution

Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-18

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 44 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Professional Botanicals, Inc. has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Professional Botanicals, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Professional Botanicals, Inc. have FDA actions?

Professional Botanicals, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0182-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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