Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2016

Every FDA drug recall initiated in 2016, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,199 recalls, newest first.

Class I · High risk

Morphine Sulfate 0.5 mg/mL

Super-Potent Drug: Out of specification for potency results (high) were obtained for one lot of morphine sulfate Inj.

Terminated Wrong potency / content Pharmakon Pharmaceuticals NDC 45183-0322-78 D-0871-2016
Class II · Moderate risk

Alendronate Sodium Tablets

Failed Impurities/Degradation Specifications: Observed levels of highest unknown impurity exceeding specification limit at the 3 month stability time point.

Terminated Impurity / degradation Sun Pharma Global Fze NDC 41616-638-68 D-0735-2016
Class II · Moderate risk

TEARS Naturale FREE

Lack of Assurance of Sterility: Some single-use vials may be filled with water rather than the product solution and the firm cannot guarantee the sterility of the water-filled vials.

Terminated Sterility / contamination Alcon Research, Ltd. D-0666-2016
Class II · Moderate risk

Medicated Better Braids

Microbial Contamination of a Non-Sterile Products: The product had a positive Staphylococcus aureus test result.

Terminated Microbial contamination Keystone Laboratories Inc D-0726-2016
Class II · Moderate risk

Tudorza Pressair

Defective Delivery System: Some units have actuation counters set to a number other than 60.

Terminated Packaging defect AstraZeneca Pharmaceuticals LP D-0781-2016
Class III · Low risk

Oxygen

CGMP Deviations: Cylinders filled using out of date gauges.

Terminated cGMP deviation Medical Park Homecare, Inc D-0776-2016
Class II · Moderate risk

Paricalcitol Capsules

Failed Impurities/Degradation Specifications: Out of specification test results for impurities during stability testing.

Terminated Impurity / degradation Teva Pharmaceuticals USA NDC 0093-7656-56 D-0774-2016

Recalls by year