epa_echo
1 records
fda
6 records
FDA Drug Recall: PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser
2024-03-06
Class II — CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
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FDA Drug Recall: PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antisept
2024-03-06
Class II — CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
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FDA Drug Recall: 7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent,
2024-03-06
Class II — CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
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FDA Drug Recall: PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser
2024-03-06
Class II — CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
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FDA Drug Recall: 7 Eleven FOR GAS ISLAND USE ONLY, Hand Sanitizer, Ethanol 70% v/v Antiseptic, Mo
2024-03-06
Class II — CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
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FDA Drug Recall: Seatex Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Soluti
2023-05-10
Class II — Superpotent Drug and Failed Impurities/Degradation Products: formula does not adhere to the labeled specifications
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