Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Jun 20, 2012 (14 years ago)

Little Remedies For Tummys

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

What was recalled

Little Remedies For Tummys, Stimulant Laxative (sennosides) Drops, 1 FL OZ (30 mL), Dist. by Medtech Products Inc., Irvington, NY 10533, UPC 7 56184 12071 2.

Drug: Sennosides

Recalling firm
Medtech Products, Inc.
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1673-2012 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Sennosides recalls

See all
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

Other recalls by Medtech Products, Inc.

All 2012 recalls
Class II · Moderate risk

Clear Eyes Redness Relief Hand Pocket Pal Tray Display

CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.

Terminated cGMP deviation Medtech Products, Inc. D-1835-2019
Class II · Moderate risk

Clear eyes REDNESS RELIEF

CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.

Terminated cGMP deviation Medtech Products, Inc. D-1834-2019