RecallHawk
Class II Recall

Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health and help Modulate Immunity 2 Fl. Oz. (60ml

Bomunity Ltd Co

Summary

The FDA issued a Class II for Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health an by Bomunity Ltd Co. Reason: Potential to be contaminated with bacteria.

Details

Source

Food Recall

External ID

F-0817-2021

Action Date

2021-08-11

Status

Terminated

Category

food

Product Description

Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health and help Modulate Immunity 2 Fl. Oz. (60ml) packaged in dark glass bottle 12 bottles per case UPC 64395 00001

Lot/Code Info: LOT 210402

Quantity Affected: 3540 cases

Reason for Recall

Potential to be contaminated with bacteria

Distribution

Nationwide throughout the US

Type: Voluntary: Firm initiated

Recall Initiated: 2021-06-04

Company

Bomunity Ltd Co

Amarillo, TX

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 59 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Bomunity Ltd Co) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bomunity Ltd Co have FDA actions?

This is the only FDA action we have on record for Bomunity Ltd Co in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0817-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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