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

18,003 recalls, newest first

Class II · Moderate risk

Gabapentin Capsules

Failed Tablet/Capsule Specifications: Complaints of empty capsules received.

Terminated Failed specification Aurobindo Pharma USA Inc NDC 16714-662-01 D-0330-2015
Class II · Moderate risk

Obagi Nu-Derm Clear

Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled bottles were inadvertently introduced into the Obagi Exfoderm Forte packaging line. Therefore customers which ordered Clear RX actually had contents of Exfoderm forte.

Terminated Labeling / mix-up Obagi Medical Products NDC 62032-101-36 D-0234-2015
Class I · High risk

1% LIDOCAINE HCl Injection

Presence of particulate matter: A returned customer sample was evaluated and found to have human hair attached to a pinched area of the stopper.

Terminated Particulate / foreign matter Hospira Inc. NDC 0409-4279-02 D-0391-2015
Class III · Low risk

Candesartan Cilexetil Tablets

Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.

Terminated Impurity / degradation Apotex Inc. NDC 60505-3621-3 D-0244-2015
Class III · Low risk

Candesartan Cilexetil Tablets

Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.

Terminated Impurity / degradation Apotex Inc. NDC 60505-3620-3 D-0243-2015
Class III · Low risk

Candesartan Cilexetil Tablets

Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.

Terminated Impurity / degradation Apotex Inc. NDC 60505-3619-3 D-0242-2015
Class III · Low risk

Candesartan Cilexetil Tablets

Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.

Terminated Impurity / degradation Apotex Inc. NDC 60505-3618-3 D-0241-2015
Class II · Moderate risk

Cyproheptadine HCl Syrup

Failed Impurities/Degradation Specifications : Out-of-specification result for an unidentified impurity at the 12 month stability test point.

Terminated Impurity / degradation Pharmaceutical Associates Inc NDC 0121-4788-10 D-0240-2015
Class II · Moderate risk

Tri-mix #4

Lack of Assurance of Sterility: A recent FDA inspection of Vann Healthcare Services facility revealed deficiencies that raise concerns about the pharmacy's ability to consistently assure sterility of their products.

Terminated Sterility / contamination Vann Healthcare Services Inc D-0312-2015
Class II · Moderate risk

Lidocaine 4% Syr

Lack of Assurance of Sterility: A recent FDA inspection of Vann Healthcare Services facility revealed deficiencies that raise concerns about the pharmacy's ability to consistently assure sterility of their products.

Terminated Sterility / contamination Vann Healthcare Services Inc D-0311-2015
Class II · Moderate risk

Epinephrine 1:1000

Lack of Assurance of Sterility: A recent FDA inspection of Vann Healthcare Services facility revealed deficiencies that raise concerns about the pharmacy's ability to consistently assure sterility of their products.

Terminated Sterility / contamination Vann Healthcare Services Inc D-0310-2015
Class II · Moderate risk

Hydroxyprogesterone Caproate

Lack of Assurance of Sterility: A recent FDA inspection of Vann Healthcare Services facility revealed deficiencies that raise concerns about the pharmacy's ability to consistently assure sterility of their products.

Terminated Sterility / contamination Vann Healthcare Services Inc D-0309-2015
Class II · Moderate risk

Sterile Water for Injection

Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.

Terminated Sterility / contamination Hospira Inc. NDC 0409-7990-09 D-0287-2015
Class II · Moderate risk

0.45% Sodium Chloride Injection

Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.

Terminated Sterility / contamination Hospira Inc. NDC 0409-7985-09 D-0286-2015
Class II · Moderate risk

0.9% Sodium Chloride Injection

Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.

Terminated Sterility / contamination Hospira Inc. NDC 0409-7983-09 D-0285-2015
Class II · Moderate risk

Lactated Ringer's Injection

Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.

Terminated Sterility / contamination Hospira Inc. NDC 0409-7953-09 D-0283-2015
Class II · Moderate risk

5% Dextrose Injection

Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.

Terminated Sterility / contamination Hospira Inc. NDC 0409-7922-09 D-0279-2015
Class II · Moderate risk

Assured Naproxen Sodium Tablets

Correct Labeled Product Mispacked; correct labeled bottles of Assured Ibuprofen softgels were packaged into cartons of Assured Naproxen Sodium Tablets, USP

Terminated Labeling / mix-up Contract Packaging Resources Inc. D-0248-2015
Class III · Low risk

TORISEL Kit

Crystallization: Impurities in a raw material used to manufacture the diluent can cause the formation of crystals in the diluent vials after cold storage. The TORISEL vials are not affected by this issue.

Terminated Failed specification Pfizer Inc. NDC 0008-1179-01 D-0235-2015

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