Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
Revive Organics, Inc.

Revive Organics, Inc. Recalls

All product recalls associated with Revive Organics, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

34

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 5201–5220 of 21320 recalls

Revie Raspberry Mango Smoothie (Revive Organics) – Norovirus Risk (2022)

Potential norovirus from IQF raspberries that were used as an ingredient in the products.

Class IIModerate

FDAJun 11, 2022CA, IL, IN +2 more• Revive Organics, Inc.

Revie Coconut Cream Smoothie (Revive Organics) – Norovirus Risk (2022)

Potential norovirus from IQF raspberries that were used as an ingredient in the products.

Class IIModerate

FDAJun 11, 2022CA, IL, IN +2 more• Revive Organics, Inc.

Revie Heart Beet Smoothie (Revive Organics) – Norovirus Risk (2022)

Potential norovirus from IQF raspberries that were used as an ingredient in the products.

Class IIModerate

1...259 260261262 263...1066

Page 261 of 1066Next

FDAJun 11, 2022CA, IL, IN +2 more• Revive Organics, Inc.

Revie Berry Patch Oats (Revive Organics) – Norovirus Risk (2022)

Potential norovirus from IQF raspberries that were used as an ingredient in the products.

Class IIModerate

FDAJun 11, 2022CA, IL, IN +2 more• Revive Organics, Inc.

Revie Strawberry Zen Smoothie (Revive Organics) – Norovirus Risk (2022)

Potential norovirus from IQF raspberries that were used as an ingredient in the products.

Class IIModerate

FDAJun 11, 2022CA, IL, IN +2 more• Revive Organics, Inc.

Revie Acai Twist Smoothie (Revive Organics) – Norovirus Risk (2022)

Potential norovirus from IQF raspberries that were used as an ingredient in the products.

Class IIModerate

FDAJun 11, 2022CA, IL, IN +2 more• Revive Organics, Inc.

Artis Pheno X-Ray System (Siemens) – Video Signal Loss Risk (2022)

A video signal from one of the transceivers of the Large Display may be lost. In very rare cases, both transceivers of the Large Display could potentially fail which can lead to the loss of both video signals. This issue can sporadically affect the Large Display in the examination room as well as the displays in the control room.

FDAJun 10, 2022Nationwide• Siemens Medical Solutions USA, Inc

HAIOU Needle Safety Syringe (Guangdong Haiou) – Needle Detachment Risk (2022)

Complaints received in which needle and needle holder have detached from the syringe after injection as well as needle not retracting into the syringe as per intended use, resulting in an increased risk of needle stick injury to the end user

FDAJun 10, 2022Nationwide• Guangdong Haiou Medical Apparatus Co., Ltd Nanyuan Industrial Zone, North Liusha Puning China

Zileuton Extended-Release Tablets (Lupin) - Failed Dissolution (2022)

Failed Dissolution Specifications: Out of specification test results observed in dissolution testing during long term stability study.

Class IIModerate

FDAJun 10, 2022Nationwide• Lupin Pharmaceuticals Inc.

Testosterone Cypionate Injection (Sun Pharma) - Sterility Risk (2022)

Lack of Assurance of Sterility: Manufacturing deviation which was reported due to a microbial excursion

Class IIModerate

FDAJun 10, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

CoolFit Vacuum Applicator (Zeltiq) – Adverse Event Concern (2022)

Laceration Risk

Executing a voluntary discontinuation and removal of parallel plate applicators due to an increase complaint rate for adverse event Paradoxical Hyperplasia (HP) during the 2019 to 2021 timeframe.

FDAJun 9, 2022AL, AK, AZ +49 more• Zeltiq Aesthetics, Inc

CoolCurve Vacuum Applicator (Zeltiq) – Adverse Event Concern (2022)

Laceration Risk

Executing a voluntary discontinuation and removal of parallel plate applicators due to an increase complaint rate for adverse event Paradoxical Hyperplasia (HP) during the 2019 to 2021 timeframe.

FDAJun 9, 2022AL, AK, AZ +49 more• Zeltiq Aesthetics, Inc

CoolCurve+ Vacuum Applicator (Zeltiq) – Adverse Event Concern (2022)

Laceration Risk

Executing a voluntary discontinuation and removal of parallel plate applicators due to an increase complaint rate for adverse event Paradoxical Hyperplasia (HP) during the 2019 to 2021 timeframe.

FDAJun 9, 2022AL, AK, AZ +49 more• Zeltiq Aesthetics, Inc

CoolMax Vacuum Applicator (Zeltiq) – Adverse Event Concern (2022)

Laceration Risk

Executing a voluntary discontinuation and removal of parallel plate applicators due to an increase complaint rate for adverse event Paradoxical Hyperplasia (HP) during the 2019 to 2021 timeframe.

FDAJun 9, 2022AL, AK, AZ +49 more• Zeltiq Aesthetics, Inc

CoolCore Vacuum Applicator (Zeltiq) – Adverse Event Concern (2022)

Laceration Risk

Executing a voluntary discontinuation and removal of parallel plate applicators due to an increase complaint rate for adverse event Paradoxical Hyperplasia (HP) during the 2019 to 2021 timeframe.

FDAJun 9, 2022AL, AK, AZ +49 more• Zeltiq Aesthetics, Inc

SnoreStop NasoSpray (Green Pharma) - Microbial Contamination (2022)

Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.

FDAJun 9, 2022Nationwide• Green Pharmaceuticals, Inc.

Wawa Cold Brew Coffee (Royal Ice Cream) – Undeclared Peanuts (2022)

Undeclared Nuts

Product is being recalled due to undeclared peanuts.

FDAJun 7, 2022DE, FL, MD +5 more• Royal Ice Cream Company

G5 School Bus (Micro Bird) – Seat Belt Component Issue (2022)

Corp. Micro Bird Inc. (Micro Bird) is recalling certain 2017-2018 G5 school buses equipped with an elevated floor and electrically adjustable driver's seat. An incorrect bracket may have been installed on the driver's seat and may interfere with the seat belt pretensioner.

NHTSAJun 6, 2022Nationwide• MICRO BIRD

Losartan Potassium 50mg (PD-Rx Pharmaceuticals) – Impurity Levels (2022)

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

Class IIModerate

FDAJun 6, 2022Nationwide• PD-Rx Pharmaceuticals, Inc.

Losartan Potassium Tablets (PD-Rx Pharmaceuticals) – CGMP Impurity Deviation (2022)

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

Class IIModerate

FDAJun 6, 2022Nationwide• PD-Rx Pharmaceuticals, Inc.