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
/
Olympus Corporation of the Americas

Olympus Corporation of the Americas Recalls

All product recalls associated with Olympus Corporation of the Americas.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 1341–1360 of 17592 recalls

Everest Bipolar Cutting Forceps (Olympus) – Packaging Breach (2024)

Fractures and breakages in packaging trays and Tyvek covers, which may result in a sterility breach

High

FDAJul 1, 2024Nationwide• Olympus Corporation of the Americas

2025 Coachmen Cross Trail (Coachmen) – Ladder Installation Problem (2024)

Forest River, Inc. (Forest River) is recalling certain 2024-2025 Cross Trail motorhomes. The ladder receiver may have been incorrectly installed without the backer, which can cause the ladder to detach.

High

NHTSAJun 28, 2024Nationwide• COACHMEN

2025 Coachmen Cross Trail (Coachmen) – Ladder Receiver Issue (2024)

Forest River, Inc. (Forest River) is recalling certain 2024-2025 Cross Trail motorhomes. The backer on the ladder receiver may not have been installed, which can cause the ladder to detach.

High

NHTSA

1...66 676869 70...880

Page 68 of 880Next

Jun 28, 2024

Nationwide

• COACHMEN

Co-op Cycles REV Bicycles (REI) – fall injury hazard (2024)

This recall involves REI Co-op Cycles REV 12-, 16-, or 20-inch kid's bicycles (all model years 2022-2024). Serial numbers included in the recall begin with "ET22," "ET23," "01VX" or "07VX." The serial number is printed underneath the bike frame on the bottom bracket or down tube. Brand Model SKU/Article # Color Co-op Cycles REV 12 Kids Bike 190741 BONDI (green) Co-op Cycles REV 12 Kids Bike 190741 PENCIL (yellow) Co-op Cycles REV 16 Kids Bike 190742 SURFS UP (blue) Co-op Cycles REV 16 Kids Bike 190742 CATCH UP (red) Co-op Cycles REV 16 Kids Bike 190743 FOUR LEAF (green) Co-op Cycles REV 20 Kids Bike 190743 PLUM BURST (purple)

Moderate

CPSCJun 27, 2024Nationwide• RECREATIONAL EQUIPMENT INC. (REI), of Sumner, Washington

Daikin FIT Heat Pumps (Daikin) – potential equipment failure (2024)

This recall involves Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps that provide heating and cooling. The recalled units are beige and the model name is printed on the outside of the unit. The model number is located on the serial plate on the side of the unit. The following model numbers are included in this recall: Recalled Daikin FIT Recalled Amana S-Series Recalled Goodman SD DZ6VSA1810-AA ASZS601810-AA GSZS601810-AB DZ6VSA1810-AB ASZS601810-AB GSZS602410-AB DZ6VSA2410-AA ASZS602410-AA GSZS603010-AB DZ6VSA2410-AB ASZS602410-AB GSZS603610-AB DZ6VSA241E-AB ASZS60241E-AB DZ6VSA3010-AA ASZS603010-AA DZ6VSA3010-AB ASZS603010-AB DZ6VSA3610-AA ASZS603610-AA DZ6VSA3610-AB ASZS603610-AB

Moderate

CPSCJun 27, 2024Nationwide• Daikin Comfort Technologies Manufacturing L.P., of Houston, Texas

Premo Turkey & Swiss (Lipari Foods) – Salmonella Contamination (2024)

Salmonella

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Premo King Club Footlong (Lipari Foods) – Salmonella Contamination (2024)

Salmonella

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Premo Meat Lovers (Lipari Foods) – Salmonella Contamination (2024)

Salmonella

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Ventana Anti-CD10 Antibody (Ventana) – Staining Inaccuracy (2024)

Their is a potential for high background and off-target staining when using the monoclonal primary antibody which can result in false positive results.

Low

FDAJun 27, 2024Nationwide• Ventana Medical Systems, Inc.

ARTIS Angiography System (Siemens) – Detector Potential Issue (2024)

A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.

Moderate

FDAJun 26, 2024Nationwide• Siemens AG/Siemens Healthcare GmbH Rittigfeld 1 Forchheim Germany

DVOT SARS-CoV-2 Antigen Test (Feng Chun Yuan) – Unauthorized Sales (2024)

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Low

FDAJun 26, 2024Nationwide• FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN) CO., LTD No. 1304 Science And Technology Innovation Park, Shajing Dahong Shenzhen China

DVOT Multi-Pathogen Antigen Test (Feng Chun Yuan) – Unauthorized Sales (2024)

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Low

FDAJun 26, 2024Nationwide• FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN) CO., LTD No. 1304 Science And Technology Innovation Park, Shajing Dahong Shenzhen China

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.

Low

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

DVOT SARS-CoV-2 Antigen Test (Feng Chun Yuan) – Unauthorized Sales (2024)

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Low

FDAJun 26, 2024Nationwide• FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN) CO., LTD No. 1304 Science And Technology Innovation Park, Shajing Dahong Shenzhen China

Tech Medical Endo Retrieval Pouch (Unimax) – Tube Fall Risk (2024)

The tube may fall into the surgical site during the grasping process.

High

FDAJun 25, 2024Nationwide• UNIMAX MEDICAL SYSTEMS INC 8F-2, NO

NIM Vital Nerve Monitoring System (Medtronic) – False Negative Risk (2024)

Potential for false negative response on the NIM Vital Nerve Monitoring System

Moderate

FDAJun 24, 2024Nationwide• Medtronic Xomed, Inc.

ESG-410 Electrosurgical Generator (Olympus) – Power-On Failure (2024)

Electrosurgical Generators ESG-410 does not power on upon use, may result in delays in initiating treatment or prolonged surgery

High

FDAJun 21, 2024Nationwide• Olympus Corporation of the Americas

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

Handset with Communicator (Medtronic) - Pairing Issue (2024)

A subset of the handsets within the kit may not be able to complete the pairing process with the communicator upon initial setup.

Moderate

FDAJun 17, 2024Nationwide• Medtronic Neuromodulation

SIGNA UHP (GE Medical) - B1+RMS Value Limit (2024)

GE HealthCare has become aware that for certain MR systems, the system predicted B1+RMS value can exceed the B1+RMS user prescribed limit when scanning in Low SAR Mode and the following two conditions are met: 1. 2D FSE T2 FLAIR OR T2 FLAIR Propeller imaging sequence is selected, AND 2. the Optimized T2 FLAIR sequence option is turned off OR not included in the MR configuration. If this occurs, it can result in overheating of an MR conditional implant.

High

FDAJun 14, 2024Nationwide• GE Medical Systems, LLC