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Urban River Spirits

Urban River Spirits Recalls

All product recalls associated with Urban River Spirits.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 781–800 of 7756 recalls

Velvet Cocoa Caramel (Urban River) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class IIILow

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Lemon Drop Mixer (Urban River) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class IIILow

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Watermelon Lemonade Splash (Urban River Spirits) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class III

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Low

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Pear-Tini Mixer (Urban River Spirits) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class IIILow

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Blackberry Lime Mixer (Urban River) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class IIILow

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Peppered Peach Bliss (Urban River) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class IIILow

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Tropical Blackberry (Urban River) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class IIILow

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Watermelon Jalapeño Mixer (Urban River) – Unsafe Processing (2024)

Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.

Class IIILow

FDAJul 1, 2024AZ, CA, CO +9 more• Urban River Spirits

Baxter PST 500 U Surgical Table (Baxter) – Potential Device Issue (2024)

Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the PST 500 U Precision Surgical Table due to a potential issue with loose spring pins in the spindle drives. This can cause the tabletop to unexpectedly tilt or move at any time, even without active use of the surgical table. This could potentially result in unintentional patient movement during surgical procedures and/or preparation for surgical procedures, including transport.

FDAJun 28, 2024Nationwide• Baxter Healthcare Corporation

Capio SLIM Suture Device (Boston Scientific) – Capture Inconsistency (2024)

Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.

FDAJun 27, 2024Nationwide• Boston Scientific Corporation

BD Insyte Autoguard IV Catheter (BD) – Tubing Hole Risk (2024)

Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.

FDAJun 26, 2024IL• Becton Dickinson Infusion Therapy Systems, Inc.

Sevelamer Carbonate Suspension (Dr. Reddy's) – Labeling Error (2024)

Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets

Class IIILow

FDAJun 26, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

Nature's Script CBD Roll-On (Global Widget) – Menthol Subpotency (2024)

Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.

Class IIILow

FDAJun 25, 2024Nationwide• GLOBAL WIDGET LLC

Hemp Bombs CBD Pain Freeze (Global Widget) – Menthol Subpotency (2024)

Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.

Class IIILow

FDAJun 25, 2024Nationwide• GLOBAL WIDGET LLC

Hemp Bombs CBD Pain Freeze (Global Widget) – Menthol Subpotency (2024)

Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.

Class IIILow

FDAJun 25, 2024Nationwide• GLOBAL WIDGET LLC

Hemp Bombs CBD Pain Freeze (Global Widget) – Menthol Subpotency (2024)

Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.

Class IIILow

FDAJun 25, 2024Nationwide• GLOBAL WIDGET LLC

Cargo Bicycles (Babboe B.V.) – Fall Hazard (2024)

This recall involves all models of two-wheeled and three-wheeled, electric and non-electric (traditional) Babboe cargo bicycles. The recalled cargo bikes are intended for (urban) transport of children, pets and/or light goods.

CPSCJun 20, 2024Nationwide• Babboe B.V., of the Netherlands

BioFire Blood Culture Panel (BioFire) – False Positive Concern (2024)

If blood culture identification panel is used in conjunction with specific lots of culture media bottles, then false positive Serratia marcescens results may occur, due to an increased level of non-viable organism from serratia marcescens targets in culture media bottles, false positive result may lead to an inappropriate change in patient therapy.

FDAJun 19, 2024Nationwide• BioFire Diagnostics, LLC

Venlafaxine Hydrochloride (Major Pharmaceuticals) – Dissolution Failure (2024)

Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.

Class IIModerate

FDAJun 18, 2024Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Afinion 2 Analyzer (Abbott) - Complexity Configuration (2024)

Five Afinion 2 (AF2) Analyzer were incorrectly market configured as Moderate Complexity and distributed to customers. Use of moderately complex assays by waived laboratories could result in erroneous results.

FDAJun 17, 2024Nationwide• Abbott Diagnostics Technologies AS Kjelsasveien