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Graviti Pharmaceuticals Private Limited

Graviti Pharmaceuticals Private Limited Recalls

All product recalls associated with Graviti Pharmaceuticals Private Limited.

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Recall Summary

Total Recalls

451

Past Year

Class I (Serious)

Most Recent

Sep 2025

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 1–20 of 451 recalls

Bupropion XL Tablets (Graviti) – Tablet Specification Failure (2025)

Failed Tablet/Capsule Specifications

Class IIModerate

FDASep 15, 2025Nationwide• Graviti Pharmaceuticals Private Limited

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.

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

Sonesta 6210 Fluoroscopy Table (Sonesta) – Weld Bracket Weakness (2025)

Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.

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FDAAug 22, 2025NH• Sonesta Medical AB Industrivagen

Heartstring Proximal Seal System (Maquet) – Deployment Failure (2025)

Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.

FDAAug 15, 2025Nationwide• Maquet Cardiovascular, LLC

Vasoview Hemopro 3 System (Maquet) – out-of-box failure (2025)

Reports of out-of-box failures discovered during the limited launch phase. Failure modes included angled deformity at the attachment site of the Harvesting Tool Jaws and the distal end of the Harvesting Tool Shaft, jaws not fully closed out of box, and heater wire lifted/flexed away from jaws.

FDAAug 6, 2025Nationwide• Maquet Cardiovascular, LLC

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.

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

Servo-u MR Ventilator (Maquet) – Patient Circuit Test Error (2025)

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

FDAMay 30, 2025Nationwide• Maquet Critical Care AB Rontgenvagen

Servo-u Ventilator (Maquet) – Patient Circuit Test Error (2025)

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

FDAMay 30, 2025Nationwide• Maquet Critical Care AB Rontgenvagen

Servo-n Ventilator (Maquet) – Patient Circuit Test Error (2025)

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

FDAMay 30, 2025Nationwide• Maquet Critical Care AB Rontgenvagen

CDI OneView BPM Probe (Terumo) – Temperature Measurement Error (2025)

Due to an error in assembly of the thermistor within some units, the affected probes will experience inaccuracy in measured shunt sensor temperature. Additionally, following changes in patient temperature without an in vivo recalibration, affected probes may experience inaccuracy in other measured parameters, including pCO2, pO2, pH, Potassium and calculated parameters, including BE, Bicarbonate, Arterial Oxygen Saturation, Delivered Oxygen, Area Under of the Curve of Delivered Oxygen, Oxygen Consumption, and Oxygen Extraction Ratio, which utilize temperature as an input. Inaccurate data may lead to inappropriate user response.

FDAMay 28, 2025Nationwide• Terumo Cardiovascular Systems Corporation

HemoClue Hemotrol Control (Mckesson) – Cold Chain Disruption (2025)

transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.

FDAApr 24, 2025Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233