PlainRecalls
FDA Drug Moderate Class II Terminated

VenomX, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottles, Skin Protectant Phillips Company, Millerton, OK -- NDC 43074-207-01

Reported: July 12, 2017 Initiated: June 8, 2017 #D-0952-2017

Product Description

VenomX, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottles, Skin Protectant Phillips Company, Millerton, OK -- NDC 43074-207-01

Reason for Recall

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Details

Recalling Firm
Phillips Co.
Units Affected
20-50 bottles/units
Distribution
Nationwide and United Kingdom
Location
Millerton, OK

Frequently Asked Questions

What product was recalled?
VenomX, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottles, Skin Protectant Phillips Company, Millerton, OK -- NDC 43074-207-01. Recalled by Phillips Co.. Units affected: 20-50 bottles/units.
Why was this product recalled?
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 12, 2017. Severity: Moderate. Recall number: D-0952-2017.