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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 6,801–6,820 of 17,964 drug recalls

Drug Recall Terminated Historical recordClass II

Kali Sulphuricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64196 5.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Terminated Historical recordClass II

Kali Phosphoricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64195 8.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Terminated Historical recordClass II

Kali Muriaticum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64194 1.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Terminated Historical recordClass II

Ferrum Phosphoricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64198 9.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Terminated Historical recordClass II

Cell Salts Combination 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64200 9.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Terminated Historical recordClass II

Calcarea Sulphurica 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64190 3.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Terminated Historical recordClass II

Calcarea Phosphorica 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64189 7.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Terminated Historical recordClass II

Calcarea Fluorica 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64188 0.

by Washington Homeopathic Products, Inc.

Reason
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Recall initiated
November 8, 2019
Reported by FDA
November 27, 2019
Distribution
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

View recall →

Drug Recall Completed Historical recordClass II

Clear Eyes Redness Relief (Little Drug),Product Size: 0.2 FL. Oz., UPC#: 7-92554-70103-7

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Clear Eyes Redness Relief (Handy Pocket Pal), Product Size: 0.2 FL. Oz., UPC#: 6-78112-15418-7

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Clear Eyes Redness Relief, Product Size: 15 mL, UPC#: 6-78112-25415-6

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Grandall Oftal-Mycin Ophthalmic Ointment, Product Size: 3.5 g

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Grandall Colirio Oftal-Mycin Redness Relief Eye Drops, Product Size: 15mL

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

FreshKote Lubricant Eye Drops, Product Size: 15 mL, NDC 15821-101-15

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

OCuSOFT retaine NaCl Ophthalmic Ointment, Product Size: 3.5g, SKU #: 777-3-77

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

OCuSOFT retaine NaCl Ophthalmic Ointment, Product Size: 3.5g, SKU #: 777-3-76

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Nano Tears XP Clear Emollient Lubricant Gel Drops twin pack, Product Size: 2 x 10 mL, Mfd. by: Altaire Pharmaceuticals, Inc., Aquebogue, NY 11931, NDC 59390-143-51

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Nano Tears MXP Forte Clear Emollient Lubricant Gel Drops, Twin Pack 2 x 10 mL, Mfd. by: Altaire Pharmaceuticals, Inc., Aquebogue, NY 11931, NDC 59390-144-51

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Altaire Ciprofloxacin HCl Ophthalmic Solution, 0.3%, 5 mL, NDC 59390-217-05

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

CVS Health Multi-Action Relief Drops, Item#: 694954, 15 mL, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.