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Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India Recalls

All product recalls associated with Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

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 141–160 of 4099 recalls

Carescape Central Station (Wipro GE Healthcare) – System Failure (2025)

GE HealthCare has identified an issue affecting Carescape" Central Station (CSCS) with software version V3.0.5, which can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs only when the number of central stations connected to the network is 118, 119 or 120.

High

FDASep 5, 2025Nationwide• Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

XERF EFFECTOR 60 (Lutronic) – Manufacturing Defects (2025)

Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.

Moderate

FDASep 4, 2025Nationwide• Lutronic Corporation 219 Sowon-Ro; Deogyang Goyang Korea (the Republic of)

Neuroquell Supplement (Atlantic) – cGMP Violations (2025)

cGMP violations

1...6 789 10...205

Page 8 of 205Next

Class IIModerate

FDAAug 27, 2025Nationwide• Atlantic Management Resources Ltd.

Honey Balsamic Dressing (Latitude 36) – undeclared soy/sesame (2025)

Undeclared Soy

Product contains undeclared Soy and Sesame

Class IHigh

FDAAug 21, 2025CA, IN• Latitude 36 Foods

Sand Bar Frozen Shrimp (Southwind Foods) – cesium contamination (2025)

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)

Class IIModerate

FDAAug 19, 2025AL, AZ, CA +6 more• Southwind Foods LLC dba Great American Seafood Imports Co.

Frozen Cooked Shrimp (Southwind Foods) – cesium contamination (2025)

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)

Class IIModerate

FDAAug 19, 2025AL, AZ, CA +6 more• Southwind Foods LLC dba Great American Seafood Imports Co.

CorNeat EverPatch (CorNeat Vision) – Surgical Patch Exposure (2025)

Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.

Moderate

FDAAug 18, 2025Nationwide• CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel

Aesculap Elan 4 Duraguard (Aesculap) – Mislabeling Issue (2025)

Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."

Low

FDAAug 18, 2025MO• Aesculap AG Am Aesculap-Platz 1 Tuttlingen Germany

EverPatch+ (CorNeat Vision) – Surgical Patch Exposure (2025)

Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.

Moderate

FDAAug 18, 2025Nationwide• CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel

RayStation Software (RaySearch) – UID uniqueness (2025)

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Low

FDAAug 8, 2025Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

ViziShot 2FLEX Needle (Olympus) – tip deformity (2025)

Potential for undetected, deformed a-traumatic tips.

Moderate

FDAAug 6, 2025Nationwide• Olympus Corporation of the Americas

Raman Spectrometers (Wasatch Photonics) – laser safety (2025)

Two new potential laser safety failure modes have been identified in the product design. Overcurrent of laser diode, and a fail-unsafe mode. The failure modes have never been found to occur in these models, whether in the field or factory, but could potentially occur under excessive force or extreme, continuous vibration.

Moderate

FDAAug 4, 2025Nationwide• WASATCH PHOTONICS

Ojasvita Chocomalt (Sri Sri Tattva) – Undeclared Soy (2025)

Undeclared Soy

Product contains undeclared soy lecithin.

Class IIModerate

FDAAug 1, 2025CA, GA, IL +7 more• SRI SRI TATTVA

Charge Plus Multi-Tools (Leatherman) – Laceration Hazard (2025)

Laceration Risk

This recall involves Leatherman Charge Plus and Charge Plus TTi multi-tools. The Charge Plus multi-tools come in black and stainless-steel colors and with a black MOLLE or black nylon sheath. The Charge Plus TTi multi-tools were sold in a stainless-steel color with a black nylon sheath. The name "Leatherman" is etched on the product.

Moderate

CPSCJul 31, 2025Nationwide• Leatherman Tool Group Inc., of Portland, Oregon

Clearview Strep A Kit (Mckesson) – classification error (2025)

Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices.

Low

FDAJul 30, 2025Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Fortress Introducer Sheath (Contract Medical) – labeling error (2025)

Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.

Low

FDAJul 30, 2025Nationwide• Contract Medical International GmbH Lauensteiner Str. 37 Dresden Germany

Ortoma Inserter Adapter (Ortoma) – weld breakage (2025)

Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

Moderate

FDAJul 28, 2025Nationwide• ORTOMA AB Falkenbergsgatan 3 Goteborg Sweden

Electrosurgical Generator (Olympus) – system error (2025)

Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.

Moderate

FDAJul 25, 2025Nationwide• Olympus Corporation of the Americas

Georgia Pine Turpentine (Diamond G) – ingestion risk (2025)

This recall involves 100% pure gum spirits of turpentine bottles. The 4-ounce, clear glass bottles are round and have a label with "Georgia Pine Gum Spirits of Turpentine" and "Diamond G Forest Products" printed on it.

High

CPSCJul 24, 2025Nationwide• Diamond G Forest Products LLC, of Patterson, Georgia

TOPS Inserter (Premia Spine) – Missing Pin Risk (2025)

Potential for missing pins at tip of inserter.

Moderate

FDAJul 16, 2025Nationwide• PREMIA SPINE LTD Giborey Israel 7 Ramat Poleg Netanya Israel