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

1,055 recalls · Class II, 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 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 II · Moderate risk

Glimepiride Tablets

Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.

Terminated Stability / shelf life Micro Labs Usa, Inc S NDC 42571-101-01 D-0046-2015

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