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Somerset Therapeutics Private Limited

Somerset Therapeutics Private Limited Recalls

All product recalls associated with Somerset Therapeutics Private Limited.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 1681–1700 of 37661 recalls

Haloperidol Decanoate Injection (Somerset) – Sterility Risk (2025)

Lack of Assurance of Sterility: Media fill with bacterial contamination

Class IIModerate

FDAMar 21, 2025Nationwide• Somerset Therapeutics Private Limited

Haloperidol Decanoate Injection (Somerset) – Sterility Risk (2025)

Lack of Assurance of Sterility: Media fill with bacterial contamination

Class IIModerate

FDAMar 21, 2025Nationwide• Somerset Therapeutics Private Limited

Haloperidol Decanoate Injection (Somerset) – Sterility Risk (2025)

Lack of Assurance of Sterility: Media fill with bacterial contamination

Class II

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Moderate

FDAMar 21, 2025Nationwide• Somerset Therapeutics Private Limited

CareStation 650 A1 (GE Healthcare) – ventilation ineffective (2025)

GE HealthCare has become aware that certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.

Moderate

FDAMar 21, 2025Nationwide• GE Medical Systems China Co., Ltd. Dev. Zone National Hi-Tech; No.

Connex Vital Signs Monitor (Baxter) – undeclared rubber band (2025)

Undeclared Allergen

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Low

FDAMar 21, 2025Nationwide• Baxter Healthcare Corporation

OEC Elite (GE Medical) – X-ray field distance issue (2025)

OEC Elite and OEC 3D Mobile C-Arms Exceeding 4% Source to Image Distance in X-ray Field.

Low

FDAMar 21, 2025Nationwide• GE Medical Systems, LLC

CareStation 750c A1 (GE Healthcare) – ventilation ineffective (2025)

Moderate

FDAMar 21, 2025Nationwide• GE Medical Systems China Co., Ltd. Dev. Zone National Hi-Tech; No.

Woolite Delicates Detergent (Reckitt) – bacterial exposure (2025)

This recall involves 50-fluid-ounce bottles of Woolite Delicates detergent (SKU 62338-72724) with lot codes S24364, S24365 and S24366, sold exclusively on Amazon.com. The lot code is printed at the top of the back of the bottle. The bottles are white with a light pink label and cap.

Moderate

CPSCMar 20, 2025Nationwide• Reckitt Benckiser LLC, of Parsippany, New Jersey

10 Drawer Dressers (GIKPAL) – tip-over risk (2025)

This recall involves GIKPAL 10 drawer dressers with model number HI1318_13. The dressers were sold in rustic brown with black handles and black sides and back. The dressers measure about 11.8 inches wide, 38.9 inches long and 39.4 inches tall, and weigh about 36 pounds. The model number "HI1318_13," "Fabric Dresser" and "Made in China" are printed on the product packaging.

High

CPSCMar 20, 2025Nationwide• CHANGZHOUHONGDA Communication Equipment Co LTD, of China

Seagull Pro Pool Cleaner (Aiper) – fire hazard (2025)

Fire/Burn Risk

This recall involves Aiper Seagull Pro cordless robotic pool cleaners with model number ZT6001. The recalled pool vacuum cleaner weighs approximately 24 pounds and measures about 19.5 x 18.5 x 15 inches. The "Aiper" brand name is printed on the top/front of the dark gray pool vacuum cleaners. The model name and the serial number, which begins with S/N "61", are printed on the label on the bottom side of the pool vacuum.

High

CPSCMar 20, 2025Nationwide• Dongguan Yuanhong Intelligent Technology Co. Ltd., of China

DxC 500 AU Analyzer (Beckman Coulter) – calibration software error (2025)

Beckman Coulter is recalling their DxC 500 AU Clinical Chemistry Analyzer because a software error causes the analyzer to not run a requested calibration order in the following scenario: when a reagent blank or calibration is ordered during sample processing and then any of the components (R1 and/or R2) depletes to zero tests, the analyzer will not be able to complete the calibration request, and the calibration order will remain pending. No further calibration orders can be processed for any assays, and the instrument refuses to accept further sample processing order after the existing calibration curves are expired. Although in-process tests will be completed, this error can cause a delay in reporting subsequent test results. No further calibration orders can be processed for any assays which may cause a delay in reporting test results.

Low

FDAMar 20, 2025AL, CA, GA +14 more• Beckman Coulter Inc.

Alinity m System (Abbott Molecular) – liquid waste risk (2025)

The design of the Alinity m System Solutions drawer enclosure may allow liquid (liquid waste or system solutions) originating in the System Solutions drawer to flow beyond the footprint of the instrument and into the walking-path of the user.

Low

FDAMar 20, 2025Nationwide• Abbott Molecular, Inc.

Cerene Cryotherapy Device (Channel Medsystems) – gasket seal issue (2025)

Due to evaporator gasket not sealing which can cause liquid nitrous oxide to drip/leak from the bottom of the device handle during treatment or after treatment during venting of the device

Moderate

FDAMar 20, 2025Nationwide• Channel Medsystems, Inc.

GenetiSure Dx Kit (Agilent) – DNA labeling component (2025)

DNA Labeling Kit for use in sample labeling to be hybridized to oligonucleotide microarrays has a component, Human Reference DNA Female aliquot, affected by a mosaic aberration that may result in Chromosome 12 baseline shift, which may lead to false positive/negative results, resulting in diagnosis delay, and may lead to delayed treatment of a treatable genetic disorder.

Low

FDAMar 20, 2025MA• Agilent Technologies, Inc.

epoc BGEM Crea Test Card (Siemens) – pH result discrepancy (2025)

The occurrence of discrepant high pH results in samples introduced with higher injection volumes with epoc sensor configuration 45.n.

Low

FDAMar 19, 2025Nationwide• Siemens Healthcare Diagnostics Inc

epoc BGEM BUN Test Card (Siemens) – pH result discrepancy (2025)

The occurrence of discrepant high pH results in samples introduced with higher injection volumes with epoc sensor configuration 45.n.

Low

FDAMar 19, 2025Nationwide• Siemens Healthcare Diagnostics Inc

Quantum Informatics VIPER (Spectrum Medical) – FDA clearance (2025)

Medical device software marketed without FDA clearance .

Low

FDAMar 19, 2025AL, AZ, AR +35 more• Spectrum Medical Ltd. Harrier 4, Meteor Business Park Cheltenham Road East Gloucester United Kingdom

Sterile Normal Saline (Medline) – bottle leakage issue (2025)

It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

Low

FDAMar 19, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Sterile Water (Medline) – bottle leakage issue (2025)

It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

Low

FDAMar 19, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Tesla Model X (Tesla) – incorrect air bag (2025)

Tesla, Inc. (Tesla) is recalling certain 2021-2024 Model S and 2021-2025 Model X vehicles. An air bag with the incorrect horn pad may have been installed, preventing the horn from sounding.

High

NHTSAMar 19, 2025Nationwide• TESLA