Drug Recall Records

This page shows recent human drug recall alerts sourced from the FDA. It includes current and some previously imported records, but is not a complete historical archive of all past recalls. For full historical data, visit the official FDA Drug Recalls page. Always consult a healthcare professional for medical advice.

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AllContamination / SterilityLabeling / PackagingUndeclared Ingredient
Hand Sanitizer, HSANI500ML, (Isopropyl Alcohol), 75% v/v, packaged in a) 500 mL
Date: 01/17/2023
Product: Hand Sanitizer, HSANI500ML, (Isopropyl Alcohol), 75% v/v, packaged in a) 500 mL bottle and b) 6 x 500 mL bottles per case, Thermo Fisher Scientific: Janssen Pharmaceuticalaan 3a, 2440 Geel - Belgium, 1 Reagent Lane, Fair Lawn, NJ 07410.
Company: Fisher Scientific Co., LLC
Recall Reason: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after March 31, 2022, due to FDA issued guidance to cease placing hand sanitizer product, produced under temporary approval, into the market after March 31, 2022.
Category: Class II
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HYDROMORPHONE (a) 1MG/ML IN NS, 50ML, 75 ML, 100ML, 175ML(NDC 00703-0018-01 and
Date: 12/27/2022
Product: HYDROMORPHONE (a) 1MG/ML IN NS,  50ML, 75 ML, 100ML, 175ML(NDC 00703-0018-01 and NDC 00409-2634-50) ; (b) 5MG/ML IN NS 60ML, 100ML, 250ML; pain, Rx only, used with a Curlin pump or no pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320, NDC# 00409-2634-50
Company: Sentara Infusion Services
Recall Reason: Lack of sterility assurance
Category: Class II
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GLUTATHIONE L REDUCED 100MG/ML (2ML NEBVL) INHALATION; GLUTATHIONE L REDUCED 200MG/ML (1ML
Date: 12/22/2022
Product: GLUTATHIONE L REDUCED 100MG/ML (2ML NEBVL) INHALATION; GLUTATHIONE L REDUCED 200MG/ML (1ML NEBVL) INHALATION; GLUTATHIONE L REDUCED 220MG/ML (30ML VIAL) INJECTABLE; GLUTATHIONE L REDUCED 500MG/ML (1ML VIAL) INJECTABLE; GLUTATHIONE L REDUCED 500MG/ML (2ML VIAL) INJECTABLE; GLUTATHIONE L REDUCED-PF- 200MG/ML (2ML VIAL) INJECTABLE, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.
Company: Pharmacy Innovations
Recall Reason: Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Category: Class II
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MEDROXYPROGESTERONE ACETATE 300 MG/ML Suspension, 10 mL vial, Rx only, Vital Care
Date: 10/07/2022
Product: MEDROXYPROGESTERONE ACETATE 300 MG/ML Suspension, 10 mL vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS  39402
Company: Pharmacy Plus, Inc. dba Vital Care Compounder
Recall Reason: Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Category: Class II
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fentaNYL Citrate in 0.9% Sodium Chloride, 2.5 mg per 250 mL, (10
Date: 07/25/2022
Product: fentaNYL Citrate in 0.9% Sodium Chloride, 2.5 mg per 250 mL, (10 mcg per mL) IV bags, Rx Only, SterRx, 141 Idaho Avenue, Plattsburgh, NY  12903, NDC 70324-327-02.
Company: SterRx, LLC
Recall Reason: Lack of Assurance of Sterility
Category: Class II
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QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores
Date: 06/23/2022
Product: QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Company: Family Dollar Stores, Llc.
Recall Reason: CGMP Deviations: product held outside appropriate storage temperature conditions.
Category: Class II
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Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For
Date: 01/26/2022
Product: Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Ten 1 mL Syringes per box, Rx Only, Sandoz Inc, Princeton, NJ 08540.  NDC: 0781-3299-69
Company: CARDINAL HEALTHCARE
Recall Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Category: Class II
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APAP 500 mg tablet (Acetaminophen 500 mg) Bulk Container, ULTRAtab Laboratories, Inc.,
Date: 01/26/2022
Product: APAP 500 mg tablet (Acetaminophen 500 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62959-210-00
Company: ULTRAtab Laboratories, Inc.
Recall Reason: CGMP Deviations
Category: Class II
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Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) Ingredients Ethanol and Methanol, in
Date: 11/30/2021
Product: Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) Ingredients Ethanol and Methanol, in 55-gallon drums, Aroma Release Technology, Inc., 7026 Discovery Drive, Chattanooga, TN 37416
Company: Aroma Release Technologies Inc
Recall Reason: Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
Category: Class I
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No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz
Date: 10/26/2021
Product: No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Distributed by SUPERVALU INC., Eden Prairie, MN 55344 USA. NDC 41163-703-10
Company: Perrigo Company PLC
Recall Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Category: Class II
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B COMPLEX INJ CMP-NO B12, NO LIDOCAINE INJECTABLE, Rx only, Talon Compounding
Date: 10/12/2021
Product: B COMPLEX INJ CMP-NO B12, NO LIDOCAINE  INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
Company: Vita Pharmacy, LLC dba Talon Compounding Pharmacy
Recall Reason: Lack of assurance of sterility
Category: Class II
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ALPROSTADIL 40MCG/ML INJ 40MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand
Date: 10/12/2021
Product: ALPROSTADIL 40MCG/ML INJ  40MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
Company: Vita Pharmacy, LLC dba Talon Compounding Pharmacy
Recall Reason: Lack of assurance of sterility
Category: Class II
View Details View FDA Recall Listings
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