Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2018

Every FDA drug recall initiated in 2018, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,681 recalls, newest first.

Class I · High risk

Ampicillin and Sulbactam for Injection

Presence of Particulate Matter: confirmed customer report of the presence of visible particulate matter believed to be red rubber particles from the manufacturing process of the active ingredients.

Terminated Particulate / foreign matter AuroMedics Pharma LLC NDC 55150-117-20 D-0866-2018
Class II · Moderate risk

Loxapine Capsules

GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination

Terminated Cross-contamination Mylan Institutional, Inc. (d.b.a. UDL Laboratories) NDC 51079-903-20 D-0823-2018
Class II · Moderate risk

Loxapine Capsules

GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination

Terminated Cross-contamination Mylan Institutional, Inc. (d.b.a. UDL Laboratories) NDC 51079-902-20 D-0822-2018
Class II · Moderate risk

Docetaxel injection concentrate

Superpotent drug: over-concentrated vials of Docetaxel injection concentrate 20 mg/mL may have been distributed.

Terminated Wrong potency / content Sanofi-Aventis U.S. LLC NDC 0955-1020-01 D-0804-2018
Class III · Low risk

Riomet (metformin hydrochloride oral solution)

Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this recall in response to identified labeling discrepancies in the patient literature.

Terminated Labeling / mix-up Sun Pharmaceutical Industries, Inc. NDC 10631-206-02 D-0818-2018
Class II · Moderate risk

Loxapine Capsules

CGMP Deviations

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-7050-01 D-0825-2018
Class II · Moderate risk

Loxapine Capsules

CGMP Deviations

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-7025-01 D-0824-2018
Class II · Moderate risk

Amlodipine and Benazapril HCL Capsules

cGMP Deviations; cleaning processes for equipment used to manufacture the specified batches was not followed according to procedure

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-6899-01 D-0820-2018
Class II · Moderate risk

Amlodipine and Benazapril HCL Capsules

cGMP Deviations; cleaning process for equipment used to manufacture the specified batches was not followed according to procedure

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-6896-01 D-0819-2018
Class II · Moderate risk

Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets

Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C (68¿F to 77¿F).

Terminated Labeling / mix-up Prescript Pharmaceuticals, Inc. D-0809-2018
Class II · Moderate risk

Clindamycin 300 mg capsules

Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C (68¿F to 77¿F).

Terminated Labeling / mix-up Prescript Pharmaceuticals, Inc. D-0808-2018
Class II · Moderate risk

Chlorhexidine 0.12% liquid

Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C (68¿F to 77¿F).

Terminated Labeling / mix-up Prescript Pharmaceuticals, Inc. D-0807-2018
Class II · Moderate risk

Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets

Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C (68¿F to 77¿F).

Terminated Labeling / mix-up Prescript Pharmaceuticals, Inc. D-0806-2018
Class II · Moderate risk

Clindamycin 150 mg capsules

Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C (68¿F to 77¿F).

Terminated Labeling / mix-up Prescript Pharmaceuticals, Inc. D-0805-2018
Class II · Moderate risk

Papaverine 30mg/Phentolamine 2mg/Prostaglandin 20mcg/mL

Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the aseptic production of certain injectable drug products.

Terminated Sterility / contamination Vitalab Pharmacy, Inc D-0733-2018
Class II · Moderate risk

Alprostadil 20 mcg/mL

Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the aseptic production of certain injectable drug products.

Terminated Sterility / contamination Vitalab Pharmacy, Inc D-0729-2018

Recalls by year