Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2017

Every FDA drug recall initiated in 2017, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,141 recalls, newest first.

Class II · Moderate risk

NitroGlycerin

Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.

Terminated Stability / shelf life Advanced Pharma Inc. NDC 15082-863-61 D-0119-2018
Class II · Moderate risk

NitroGlycerin

Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.

Terminated Stability / shelf life Advanced Pharma Inc. NDC 15082-863-67 D-0118-2018
Class I · High risk

NitroGlycerin

Subpotent Drug: found to be below the specification for labeled assay.

Terminated Wrong potency / content Advanced Pharma Inc. NDC 15082-863-61 D-0115-2018
Class I · High risk

NitroGlycerin

Subpotent Drug: found to be below the specification for labeled assay.

Terminated Wrong potency / content Advanced Pharma Inc. NDC 15082-863-67 D-0114-2018
Class II · Moderate risk

VenomX

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Terminated Stability / shelf life Phillips Co. NDC 43074-207-01 D-0952-2017
Class II · Moderate risk

StaphWash+Plus+ Skin Protectant

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Terminated Stability / shelf life Phillips Co. NDC 43074-101-01 D-0951-2017
Class II · Moderate risk

StingMed Insect bites Skin Protectant. Zinc acetate

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Terminated Stability / shelf life Phillips Co. NDC 04307-100-11 D-0950-2017
Class I · High risk

Andropharm M1 Alpha

Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.

Terminated Unapproved drug Andropharm, LLC D-1143-2017
Class I · High risk

Andropharm Sten Z

Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.

Terminated Unapproved drug Andropharm, LLC D-1142-2017
Class II · Moderate risk

NasalCrom (cromolyn sodium)

CGMP Deviations: Possibility of the presence of microbial contamination in the water used to manufacture this product lot.

Terminated Microbial contamination Bausch & Lomb, Inc. D-0899-2017
Class I · High risk

EliquisTablets 5mg

Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.

Terminated Labeling / mix-up Bristol-myers Squibb Company NDC 0003-0894-21 D-0959-2017

Recalls by year