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 ↗

RSS Feed

Home
/
Brands
/
K.C. Pharmaceuticals, Inc

K.C. Pharmaceuticals, Inc Recalls

All product recalls associated with K.C. Pharmaceuticals, Inc.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 4081–4100 of 25002 recalls

Original Eye Drops (K.C. Pharmaceuticals) – Manufacturing Documentation (2023)

CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.

Class IIModerate

FDAJun 13, 2023Nationwide• K.C. Pharmaceuticals, Inc

Dry Eye Relief Drops (K.C. Pharmaceuticals) – Manufacturing Documentation (2023)

CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.

Class IIModerate

FDAJun 13, 2023Nationwide• K.C. Pharmaceuticals, Inc

Ranch Salad Dressing (Tony Charchere's) – Product Spoilage (2023)

Bubbling of product and sour taste

Class III

1...203 204205206 207...1251

Page 205 of 1251Next

Low

FDAJun 13, 2023IN, LA• SCREAMING EAGLE CO PACK LLC

Ingenia Elition S MR System (Philips) – Smoke Detector Bypass (2023)

The system operator is able to bypass the SmokeDetector Interlock system locking mechanism after a smoke detection by power cycling the system.

Moderate

FDAJun 12, 2023Nationwide• Philips North America

MR 7700 Magnetic Resonance System (Philips) – Smoke Detector Bypass (2023)

The system operator is able to bypass the SmokeDetector Interlock system locking mechanism after a smoke detection by power cycling the system.

Moderate

FDAJun 12, 2023Nationwide• Philips North America

Ingenia Elition S MR System (Philips) – Smoke Detector Cable Issue (2023)

During installation of the SmokeDetector Interlock, a connecting cable, between the SmokeDetector Interlock and the host PC, may not have been properly installed. This connection is used for service diagnostics and does not impact the functionality of the system and/or the SmokeDetector Interlock system.

Moderate

FDAJun 12, 2023Nationwide• Philips North America

Oxylog 3000 Plus Ventilator (Draeger) – Power Transition Failure (2023)

Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation.

Moderate

FDAJun 12, 2023Nationwide• Draeger Medical, Inc.

Allura Xper X-ray System (Philips) – FlexMove Carriage Defect (2023)

The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

Moderate

FDAJun 12, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Azurion 7 X-ray System (Philips) – FlexMove Carriage Defect (2023)

The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

Moderate

FDAJun 12, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Ingenia Elition X MR System (Philips) – Smoke Detector Cable Issue (2023)

Moderate

FDAJun 12, 2023Nationwide• Philips North America

Ingenia Elition X MR System (Philips) – Smoke Detector Bypass (2023)

The system operator is able to bypass the SmokeDetector Interlock system locking mechanism after a smoke detection by power cycling the system.

Moderate

FDAJun 12, 2023Nationwide• Philips North America

Lysteda Tranexamic Acid Tablets (Amring) – Conductivity Specification (2023)

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Class IIILow

FDAJun 12, 2023Nationwide• Amring Pharmaceuticals Inc

Endometrin Vaginal Insert (Ferring) – Microbial Contamination Risk (2023)

cGMP deviations: potential for Microbial Contamination of Non-Sterile Products

Class IIModerate

FDAJun 12, 2023Nationwide• Ferring Pharmaceuticals Inc

MR 7700 Magnetic Resonance System (Philips) – Smoke Detector Cable Issue (2023)

Moderate

FDAJun 12, 2023Nationwide• Philips North America

Sterile Ultrasound Gel (Turkuaz) – Sterility Concern (2023)

Sterility of Ultrasound gel can not be guaranteed.

Moderate

FDAJun 9, 2023IL• Turkuaz Saglik Hizmetleri Medikal Temizlik Kim. Ur. San. ve Tic. A.S. Akcaburgaz Mahallesi Muhsin Yazicioglu Caddesi No:45/5 Esenyurt Turkey

DEKA Car Battery (East Penn Manufacturing) – Electrical Connection Issue (2023)

East Penn Manufacturing Company, Inc. (East Penn) is recalling certain Deka batteries, model 648MF. The electrical connection between the internal battery cell and external terminal may be incomplete, which can cause an electrical spark.

Moderate

NHTSAJun 9, 2023Nationwide• EAST PENN MANUFACTURING

EVIS EXERA III Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Bronchovideoscope BF Type (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Option Elite Retrievable Filter (Argon Medical) – Potential Embolism Risk (2023)

There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism.

Moderate

FDAJun 8, 2023Nationwide• Argon Medical Devices, Inc

EVIS EXERA Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas