Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2026

Every FDA drug recall initiated in 2026, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

563 recalls, newest first.

Class II · Moderate risk

Maximum

Stability Data Does Not Support Expiry Date.

Ongoing Stability / shelf life HTO Nevada Inc. dba Kirkman D-0387-2026
Class II · Moderate risk

Maximum

Stability Data Does Not Support Expiry Date.

Ongoing Stability / shelf life HTO Nevada Inc. dba Kirkman D-0386-2026
Class II · Moderate risk

Five-Star

Stability Data Does Not Support Expiry Date.

Ongoing Stability / shelf life HTO Nevada Inc. dba Kirkman D-0385-2026
Class III · Low risk

Nilotinib Capsules

Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.

Ongoing Failed specification Cipla USA, Inc. NDC 69097-032-74 D-0382-2026
Class III · Low risk

Nilotinib Capsules

Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.

Ongoing Failed specification Cipla USA, Inc. NDC 69097-031-74 D-0381-2026
Class II · Moderate risk

Semaglutide

CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution

Ongoing Microbial contamination Harbin Jixianglong Biotech Co., Ltd. NDC 84385-106-01 D-0380-2026
Class II · Moderate risk

Semaglutide

CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution

Ongoing Microbial contamination Harbin Jixianglong Biotech Co., Ltd. NDC 84385-106-01 D-0379-2026
Class II · Moderate risk

Amantadine HCl

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Ongoing Dissolution failure AvKARE NDC 50268-069-15 D-0341-2026
Class III · Low risk

Eptifibatide Injection

Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.

Ongoing Labeling / mix-up Slate Run Pharmaceuticals D-0343-2026
Class II · Moderate risk

Adbry

Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.

Ongoing Sterility / contamination Leo Pharma INC NDC 50222-350-91 D-0339-2026
Class II · Moderate risk

Dexamethasone Sodium Phosphate Injection

Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP impurity G (Impurity RU 49336) and dexamethasone formate.

Ongoing Impurity / degradation Somerset Therapeutics LLC D-0398-2026
Class III · Low risk

Pitavastatin Tablets

Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg

Ongoing Particulate / foreign matter Annora Pharma Private Limited NDC 72603-479-01 D-0391-2026

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