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Wish Isopropyl Alcohol

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CASHSN30049099
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INTELLIGENCE

Showing 5 of 5 briefs for Wish Isopropyl Alcohol
REGULATORY INTELLIGENCE·Recall

Cardinal Health's Webcol Alcohol Prep Pad Recall: A Class I Sterility Breach Demands Immediate Supply Chain Action

Cardinal Health 200, LLC has initiated a Class I recall of over 174 million boxes of Webcol Alcohol Prep pads due to *Paenibacillus phoenicis* contamination. This non-sterility event, impacting distribution across the United States, Puerto Rico, and Japan, necessitates immediate action from procurement and regulatory teams to assess inventory, mitigate patient risk, and secure alternative sterile medical supplies.

90-Day Activity
CMCatherine Morrow· Senior Regulatory Intelligence Analyst
2026-03-25 Recall
REGULATORY INTELLIGENCE·Recall

FDA Initiates Class III Recall for TopCare Health 70% Isopropyl Alcohol Due to Cross-Contamination

Consumer Product Partners, LLC has initiated a Class III recall for 60 bottles of TopCare Health 70% Isopropyl Alcohol due to cross-contamination. This event underscores critical supply chain and quality control vulnerabilities for distributors and retailers of OTC products. Procurement and regulatory teams must scrutinize supplier quality systems to mitigate similar risks and ensure product integrity.

90-Day Activity
CMCatherine Morrow· Senior Regulatory Intelligence Analyst
2025-10-01
REGULATORY INTELLIGENCE·Recall

Kroger 70% Isopropyl Alcohol Recalled Nationwide by Consumer Product Partners, LLC Over Cross-Contamination Concerns

Consumer Product Partners, LLC initiated a nationwide Class III recall (D-0660-2025) of Kroger 70% Isopropyl Alcohol due to cross-contamination. This event underscores critical supply chain vulnerabilities and the imperative for robust quality control, impacting procurement strategies and regulatory compliance for firms sourcing over-the-counter pharmaceuticals and chemicals.

90-Day Activity
MKMeera Krishnan· Senior Regulatory Intelligence Analyst
2025-10-01
REGULATORY INTELLIGENCE·Recall

FDA Initiates Class II Recall for Wuxi Medical Instrument Factory's ViaMed Alcohol Prep Pads Due to Sterility Concerns

Wuxi Medical Instrument Factory Co., Ltd. faces an FDA Class II recall for ViaMed Alcohol Prep Pads due to sterility assurance failures and cGMP deviations. This impacts Rece International Corp. and necessitates immediate supply chain review for sterile medical devices. Procurement and regulatory teams must assess exposure and reinforce supplier qualification protocols to mitigate risk.

90-Day Activity
PSPriya Subramaniam· Intelligence Analyst
2025-03-05
REGULATORY INTELLIGENCE·Recall

Zeco LLC Recalls Rubbing Alcohol (70% Isopropyl Alcohol) Over Non-Sterile Water CGMP Deviations

Zeco LLC has initiated a Class II recall for Rubbing Alcohol (70% Isopropyl Alcohol) and First-Aid Antiseptic due to critical CGMP deviations, specifically using non-sterile water in production. This impacts supply chains nationwide in the US and Canada. Procurement directors must reassess supplier qualification for antiseptic products, while regulatory affairs must ensure robust quality agreements to mitigate similar compliance risks.

90-Day Activity
PSPriya Subramaniam· Intelligence Analyst
2024-08-28