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
/
Clinical Innovations, LLC

Clinical Innovations, LLC Recalls

All product recalls associated with Clinical Innovations, LLC.

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 5081–5100 of 21320 recalls

Sweetums Preservative Free Sucrose (Clinical Innovations) – Product Defect (2022)

Firm received complaints of leaking cups, black liquid, and black particulates in the 24% Sucrose Solution.

Class IIModerate

FDAJul 19, 2022Nationwide• Clinical Innovations, LLC

Sweetums Preservative Free Solution (Clinical Innovations) – Product Defect (2022)

Firm received complaints of leaking, black liquid, and black particulates in the product vials.

Class IIModerate

FDAJul 19, 2022Nationwide• Clinical Innovations, LLC

Sweetums Sucrose Solution (Clinical Innovations) – Product Defect (2022)

Firm received complaints of leaking, black liquid, and black particulates in the product vials.

1...253 254255256 257...1066

Page 255 of 1066Next

Class IIModerate

FDAJul 19, 2022Nationwide• Clinical Innovations, LLC

BD PhaSeal Y-Site Connector (Becton Dickinson) – Incorrect Expiration (2022)

Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.

FDAJul 18, 2022Nationwide• Becton Dickinson & Company

Irbesartan Tablets (Jubilant Cadista) – Dissolution Failure (2022)

Failed Dissolution Specifications

Class IIModerate

FDAJul 18, 2022Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Irbesartan Tablets (Jubilant Cadista) – Dissolution Failure (2022)

Failed dissolution specifications.

Class IIModerate

FDAJul 18, 2022Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Dimension Vista LOCI CA 15-3 (Siemens) – Sample Bias Risk (2022)

Negative bias with patient samples. The mean patient sample bias range from -26% to -33%,potential risk of delay in appropriate treatment and management decisions.

FDAJul 18, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Fulvestrant Injection (Zydus) – Impurity Specification (2022)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAJul 15, 2022Nationwide• Zydus Pharmaceuticals (USA) Inc

Avant Hand Sanitizer (Aire-Master) – Water System Issue (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Common Sense Hand Sanitizer (Aire-Master) – Water Contamination (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Protect U Guard Hand Sanitizer (Aire-Master) – Water Quality Concerns (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Protect U Guard Hand Sanitizer (Aire-Master) – Manufacturing Deviation (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Avant Hand Sanitizer (Aire-Master) – Water Contamination (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Stage 2 Ophardt Hand Sanitizer (Aire-Master) – Production Flaw (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

cobas e801 Analyzer (Roche) – Software Signal Impact (2022)

Software issue resulting in signals and sample test results of Pre-Wash tests being impacted. The following assays are considered impacted by the issue: Anti-HAV2, Anti-HBc IgM, IGF-1, Myogloin, Rubella IgG, and Toxo IgG.

FDAJul 14, 2022Nationwide• Roche Diagnostics Operations, Inc.

EverFlex Peripheral Stent (Medtronic) – Deployment Workaround (2022)

Update to IFU provides a manual deployment workaround method to help mitigate potential harms related to partial stent deployment.

FDAJul 14, 2022Nationwide• Medtronic Inc.

Surpria 64 Software (FUJIFILM) – Scanning Error Risk (2022)

Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation

FDAJul 12, 2022Nationwide• FUJIFILM Healthcare Americas Corporation

AXIOM Sensis Systems (Siemens) – Signal Input Box Mounting (2022)

The Sensis Signal Input Box provides hooks as a milled item on the bottom of the box support the possibility of mounting the Signal Input Box on an accessory rail (e.g., at the patient table), In the event the mounting position deviates from the default position, the following are possible: Patient touching the Signal Input Box may result in a touch leakage current to the patient; Spillage of liquid entering the Signal Input Box

FDAJul 12, 2022Nationwide• Siemens Medical Solutions USA, Inc

Surpria Software (FUJIFILM) – Scanning Error Risk (2022)

Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation

FDAJul 12, 2022Nationwide• FUJIFILM Healthcare Americas Corporation

SCENARIA View Software (FUJIFILM) – Scanning Error Risk (2022)

Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation

FDAJul 12, 2022Nationwide• FUJIFILM Healthcare Americas Corporation