Dia-Ionx and Arthro-iONX Pet Supplement Recall

Arthro-iONX – Joint & Mobility Pain Formula and DIA-IONX – Blood Sugar Imbalance are being recalled due to “foul smell” and “bacterial contamination”.

9/20/2017

VETiONX
4635 40th St SE
Grand Rapids, MI 49512

Dear Customer:

This is to inform you of a product recall involving:

DIA-IONX – Blood Sugar Imbalance
4 Fluid Ounce Bottle
UPC: 891129002675
Lot# 022017F
Exp: 7/19

This recall has been initiated due to bacterial contamination and foul smell in some bottles. We have not received any health complaints; however, use of this product is not recommended.

We began shipping this product on 7/26/2017.

Immediately examine your product and determine if your product is subject to recall. If you have further distributed this product to your customers, please identify your customers and notify them at once of this product recall. Please include a copy of this letter with your customer notification. If you still have any impacted products subject to recall, you may either: 1) return them to our facility or 2) destroy them by pouring down the drain and discarding empty bottles in the trash.

Please acknowledge your completion of one of these two actions as soon as possible by either calling us at 1-866-977-0888 or emailing us at customerservice@vetionx.com and placing “Dia-Ionx Recall” in the email subject line.

If you have any questions, please contact customer service:
Email: customerservice@vetionx.com
Phone: 1-866-977-0888.

This recall is being made with the knowledge of the Food and Drug Administration.

Sincerely,

VETiONX Compliance Team

9/20/2017

VETiONX
4635 40th St SE
Grand Rapids, MI 49512

Dear Customer:

This is to inform you of a product recall involving:

Arthro-iONX – Joint & Mobility Pain Formula
4 Fluid Ounce Bottle
UPC: 891129002514
Lot# 040717A
Exp: 12/19

This recall has been initiated due to bacterial contamination and foul smell in some bottles. We have not received any health complaints; however, use of this product is not recommended.

We began shipping this product on 7/26/2017.

Immediately examine your product and determine if your product is subject to recall. If you have further distributed this product to your customers, please identify your customers and notify them at once of this product recall. Please include a copy of this letter with your customer notification. If you still have any impacted products subject to recall, you may either: 1) return them to our facility or 2) destroy them by pouring down the drain and discarding empty bottles in the trash.

Please acknowledge your completion of one of these two actions as soon as possible by either calling us at 1-866-977-0888 or emailing us at customerservice@vetionx.com and placing “Arthro-Ionx Recall” in the email subject line.

If you have any questions, please contact customer service:
Email: customerservice@vetionx.com
Phone: 1-866-977-0888.

This recall is being made with the knowledge of the Food and Drug Administration.

Sincerely,

VETiONX Compliance Team