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
/
Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa Recalls

All product recalls associated with Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

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 2761–2780 of 21320 recalls

Epix Universal Clip Applier (Applied Medical) – Clip Loading Issue (2024)

Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.

High

FDAJan 30, 2024Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Trinias Angiography System (Shimadzu) – Flat Panel Malfunction (2024)

Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.

Moderate

FDAJan 29, 2024Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

Soltive Laser (Olympus) – Non-Compliant Power Cord (2024)

A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.

Low

1...137 138139140 141...1066

Page 139 of 1066Next

FDA

Jan 29, 2024

• Olympus Corporation of the Americas

Vantage Elan MRI (Canon) – SFG Value Mismatch (2024)

For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.

Moderate

FDAJan 29, 2024Nationwide• Canon Medical System, USA, INC.

Vantage MRI Systems (Canon) – SFG Value Mismatch (2024)

Moderate

FDAJan 29, 2024Nationwide• Canon Medical System, USA, INC.

Soltive Pro Laser (Olympus) – Non-Compliant Power Cord (2024)

A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.

Low

FDAJan 29, 2024IN• Olympus Corporation of the Americas

Vantage Titan MRI (Canon) – SFG Value Mismatch (2024)

Moderate

FDAJan 29, 2024Nationwide• Canon Medical System, USA, INC.

VITROS XT 3400 System (Ortho) – QC Baseline Defect (2024)

A software defect affecting VITROS Systems running VITROS Software Versions 3.8.1 causes QC baseline statistics to not update as expected when changed by the user. This may cause erroneous patient results to be reported.

High

FDAJan 26, 2024Nationwide• Ortho-Clinical Diagnostics, Inc.

BCID2 Panel (BioFire) – False Positive Results (2024)

Due to a trend in false positive Candida tropicalis results on blood culture panel when using certain BD BACTEC vial mediums

Moderate

FDAJan 26, 2024Nationwide• BioFire Diagnostics, LLC

FilmArray GI Panel (BioFire) – False Norovirus Results (2024)

Due to potential signals of increased false positive Norovirus results when using the gastrointestinal (GI) panel.

Moderate

FDAJan 26, 2024Nationwide• BioFire Diagnostics, LLC

Nortrel Tablets (Teva) – Tablet Discoloration (2024)

Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.

Class IIILow

FDAJan 25, 2024Nationwide• Teva Pharmaceuticals USA, Inc

Febuxostat Tablets (Amerisource) – CGMP Deviation (2024)

CGMP Deviations

Class IIModerate

FDAJan 25, 2024Nationwide• Amerisource Health Services LLC

Nortrel 7/7/7 Tablets (Teva) – Tablet Discoloration (2024)

Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.

Class IIILow

FDAJan 25, 2024Nationwide• Teva Pharmaceuticals USA, Inc

Pure Care Hand Sanitizer (Alpha Aromatics) – CGMP Deviation (2024)

CGMP Deviations

Class IIModerate

FDAJan 25, 2024IN, MI, NC• Alpha Aromatics

Atellica IM EPO Assay (Siemens) – Result Bias (2024)

Siemens Healthcare Diagnostics has confirmed an average negative bias of -35% compared to the 3rd World Health Organization (WHO) International Standard (NIBSC code: 11/170) that is proportional across the assay measuring interval. The reference interval as claimed in the Instructions for Use (IFU) is not achieved with affected lots.

Moderate

FDAJan 24, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

Impression Coping (Thommen) – Canal Depth Issue (2024)

The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.

Low

FDAJan 24, 2024Nationwide• Thommen Medical AG Eschenweg 3 Bettlach Switzerland

Stay Informed

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa Recalls

Recall Summary

Epix Universal Clip Applier (Applied Medical) – Clip Loading Issue (2024)

Trinias Angiography System (Shimadzu) – Flat Panel Malfunction (2024)

Soltive Laser (Olympus) – Non-Compliant Power Cord (2024)

Vantage Elan MRI (Canon) – SFG Value Mismatch (2024)

Vantage MRI Systems (Canon) – SFG Value Mismatch (2024)

Soltive Pro Laser (Olympus) – Non-Compliant Power Cord (2024)

Vantage Titan MRI (Canon) – SFG Value Mismatch (2024)

VITROS XT 3400 System (Ortho) – QC Baseline Defect (2024)

BCID2 Panel (BioFire) – False Positive Results (2024)

FilmArray GI Panel (BioFire) – False Norovirus Results (2024)

VITROS 3600 System (Ortho) – QC Baseline Defect (2024)

VITROS 5600 System (Ortho) – QC Baseline Defect (2024)

VITROS 4600 System (Ortho) – QC Baseline Defect (2024)

VITROS XT 7600 System (Ortho) – QC Baseline Defect (2024)

Nortrel Tablets (Teva) – Tablet Discoloration (2024)

Febuxostat Tablets (Amerisource) – CGMP Deviation (2024)

Nortrel 7/7/7 Tablets (Teva) – Tablet Discoloration (2024)

Pure Care Hand Sanitizer (Alpha Aromatics) – CGMP Deviation (2024)

Atellica IM EPO Assay (Siemens) – Result Bias (2024)

Impression Coping (Thommen) – Canal Depth Issue (2024)