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.

Search
By Dosage Form:
AllTabletsCapsulesInjectables
By Recall Category:
AllContamination / SterilityLabeling / PackagingUndeclared Ingredient
Par Health and Endo USA – Argatroban Injection 250 mg/2.5 mL (100 mg/mL)
Date: 10/14/2026
Brand: Par Health and Endo USA
Product: Argatroban Injection 250 mg/2.5 mL (100 mg/mL)
Company: Par Health USA, LLC
Recall Reason: Presence of particulate matter, identified as cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steel
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Par Pharmaceutical – Brevital Sodium 500 mg/vial for Injection
Date: 10/09/2026
Brand: Par Pharmaceutical
Product: Brevital Sodium 500 mg/vial for Injection
Company: Par Health
Recall Reason: Presence of particulate matter identified as cellulose
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Greenwich – Glutathione Injection
Date: 10/01/2026
Brand: Greenwich
Product: Glutathione Injection
Company: Greenwich Rx
Recall Reason: Potential elevated endotoxin levels
Dosage Form: Injection
Category: Quality / Potency
View Details View FDA Recall Listings
ICU Medical LLC – 0.9% Sodium Chloride Injection, USP, 100 mL
Date: 09/21/2026
Brand: ICU Medical LLC
Product: 0.9% Sodium Chloride Injection, USP, 100 mL
Company: Otsuka ICU Medical LLC
Recall Reason: Product mix-up where 0.9% Sodium Chloride Injection, USP overwrap may contain 10 mEq Potassium Chloride Injection
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Par Pharmaceutical – Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) for Intravenous Infusion
Date: 09/21/2026
Brand: Par Pharmaceutical
Product: Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) for Intravenous Infusion
Company: Par Health
Recall Reason: Presence of particulate matter identified as cellulose or stopper material
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Niwali – Tejocote Capsules and Pieces
Date: 09/21/2026
Brand: Niwali
Product: Tejocote Capsules and Pieces
Company: Global Mix Inc.
Recall Reason: Products contain yellow oleander (Thevetia peruviana).
Dosage Form: Capsule
Category: Other Recall Issue
View Details View FDA Recall Listings
Centric Compounding – Compounded Glutathione 200 mg/mL 30 mL multidose vial; Myer’s Cocktail 30 mL multidose vial; Tri-Immune Boost 30 mL multidose vial
Date: 09/13/2026
Brand: Centric Compounding
Product: Compounded Glutathione 200 mg/mL 30 mL multidose vial; Myer’s Cocktail 30 mL multidose vial; Tri-Immune Boost 30 mL multidose vial
Company: Centric Compounding LLC
Recall Reason: Elevated Endotoxin level
Dosage Form: Other / Unspecified
Category: Quality / Potency
View Details View FDA Recall Listings
B. Braun – 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container
Date: 09/03/2026
Brand: B. Braun
Product: 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container
Company: B. Braun Medical Inc.
Recall Reason: Presence of particulate matter identified as iron oxide
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
American Regent, Inc. – Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial
Date: 09/03/2026
Brand: American Regent, Inc.
Product: Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial
Company: American Regent, Inc.
Recall Reason: Presence of particulate matter and lack of sterility assurance
Dosage Form: Injection
Category: Contamination / Sterility
View Details View FDA Recall Listings
Lipofit – Lipofit Extreme 2.0 Fat Burner Dietary Supplement
Date: 08/31/2026
Brand: Lipofit
Product: Lipofit Extreme 2.0 Fat Burner Dietary Supplement
Company: Ana Salazar Modela Tu Cuerpo Inc.
Recall Reason: Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)
Dosage Form: Other / Unspecified
Category: Undeclared / Unapproved Ingredient
View Details View FDA Recall Listings
Baxter – 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container
Date: 08/26/2026
Brand: Baxter
Product: 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container
Company: Baxter International Inc.
Recall Reason: Potential presence of particulate matter identified as fiberglass in the solution.
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Baxter – 70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic Container
Date: 08/25/2026
Brand: Baxter
Product: 70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic Container
Company: Baxter International Inc.
Recall Reason: Potential presence of particulate matter identified as stainless steel particles in the solution.
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
1
2
3
…
12
Next »