Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

Is Sennosides recalled?

Not under an active recall. Sennosides was recalled 17 times in the past — all now closed. Most recent: Dec 21, 2021.

Most common reason: Microbial contamination (10 of these recalls)

Recalls are matched by product description. A recall usually affects specific lots, not every package of Sennosides. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.

Sennosides recalls on record

none so far in 2026; 17 on record, newest first
Class II · Moderate risk

Senna (sennosides 8.8 mg)

Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported

Terminated Impurity / degradation Geritrex, LLC NDC 54162-007-08 D-1437-2019
Class II · Moderate risk

Senna (sennosides 8.8 mg)

Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported

Terminated Impurity / degradation Geritrex, LLC NDC 53807-556-08 D-1436-2019
Class II · Moderate risk

SDA Senna Syrup

CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.

Terminated Microbial contamination RIJ Pharmaceutical LLC NDC 66424-562-08 D-0851-2018
Class II · Moderate risk

Geritrex Senna Syrup

CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.

Terminated Microbial contamination RIJ Pharmaceutical LLC NDC 54162-007-08 D-0850-2018
Class II · Moderate risk

GeriCare Senna Syrup

CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.

Terminated Microbial contamination RIJ Pharmaceutical LLC NDC 57696-452-08 D-0848-2018
Class II · Moderate risk

RPC Senna Syrup

CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.

Terminated Microbial contamination RIJ Pharmaceutical LLC D-0844-2018
Class I · High risk

Senna Laxative

Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.

Terminated Labeling / mix-up Magno Humphries Laboratories, Inc D-0342-2018
Class II · Moderate risk

Senna Syrup

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 0904-6289-09 D-1526-2016
Class II · Moderate risk

Senexon Liquid

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 0536-1000-59 D-1525-2016
Class II · Moderate risk

Sennazon (sennosides)

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 76518-100-08 D-1520-2016
Class II · Moderate risk

Sennosides

Labeling: Label Mixup: SENNOSIDES, Tablet, 8.6 mg may have potentially been mislabeled as one of the following drugs: FEXOFENADINE HCL, Tablet, 180 mg, NDC 41167412003, Pedigree: AD62834_1, EXP: 5/23/2014; TRIMETHOBENZAMIDE HCL, Capsule, 300 mg, NDC 53489037601, Pedigree: W002976, EXP: 6/11/2014; LORATADINE, Tablet, 10 mg, NDC 45802065078, Pedigree: W003253, EXP: 6/17/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-876-2014
Class II · Moderate risk

SENNOSIDES Tablet

Labeling:Label Mixup; SENNOSIDES Tablet, 8.6 mg may be potentially mislabeled as SACCHAROMYCES BOULARDII LYO, Capsule, 250 mg, NDC 00414200007, Pedigree: AD37063_7, EXP: 5/13/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-656-2014
Class II · Moderate risk

Little Remedies For Tummys

Subpotent (Single Ingredient) Drug: This product is being recalled because of sub-potency of the sennosides.

Terminated Wrong potency / content Medtech Products, Inc. D-1673-2012