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Teligent Pharma, Inc.

Teligent Pharma, Inc. Recalls

All product recalls associated with Teligent Pharma, Inc..

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Recall Summary

Total Recalls

1000

Past Year

423

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 1521–1540 of 4598 recalls

Erythromycin Topical Gel (Teligent) – Impurities Concern (2021)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJun 22, 2021Nationwide• Teligent Pharma, Inc.

Erythromycin Topical Solution (Teligent) – Impurities Concern (2021)

Failed Impurities/Degradation Specifications

Class IIILow

FDAJun 22, 2021Nationwide• Teligent Pharma, Inc.

WOM World of Medicine AG Salzufer 8 Berlin Germany: Covidien HysteroLux Fluid Management System Control Unit,...

When the display of inflow volume to the uterus reaches 32450 ml, the fluid management system control unit display will freeze because the internal software calculation threshold is reached. The outflow measurement will continue, and so the deficit accumulated up to this point will start counting backwards to 0 ml. There is a risk of distention fluid reaching the soft tissue circulatory system.

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FDAJun 18, 2021Nationwide• WOM World of Medicine AG Salzufer 8 Berlin Germany

Gentherm Medical, LLC: Hemotherm CE Dual Reservoir Cooler/Heater, Model 400CE, 1...

There is a potential risk of device contamination and patient infection associated with the device because of the potential for organisms (including Nontuberculous mycobacteria NTM) to grow in the water systems of any heater-cooler device, and contaminated water from any heater-cooler device has the potential to aerosolize into the operating room during surgery which could lead to patient infection.

FDAJun 17, 2021Nationwide• Gentherm Medical, LLC

GE Healthcare, LLC: Revolution EVO, Optima CT660, Optima CT680 CT Systems.

Improperly loaded software options may result in additional X -ray radiation exposure to the patient.

FDAJun 14, 2021Nationwide• GE Healthcare, LLC

WALLACE FORGE MOUNT COUPLERS Equipment Recall: EQUIPMENT

Wallace Forge Company (Wallace Forge) is recalling Medium duty adjustable mount couplers part numbers R25160. The coupler may experience excessive play due to a missing .750" radius piece.

NHTSAJun 14, 2021Nationwide• WALLACE FORGE

Green Salsa (Taco Casa) – Foreign Material Risk (2021)

Potential to contain a foreign material

Class IIModerate

FDAJun 14, 2021Nationwide• Heritage Family Specialty Foods, Inc.

Hatch Verde Salsa (Heritage Family) – Foreign Material Risk (2021)

Potential to contain a foreign material

Class IIModerate

FDAJun 14, 2021Nationwide• Heritage Family Specialty Foods, Inc.

GE OEC Medical Systems, Inc: OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray Syst...

There is a potential that the coin cell battery used to monitor X-Ray tube temperature may deplete early causing the system to become inoperable.

FDAJun 10, 2021Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC Elite mobile C-arm - Product Usage: intended to provi...

There is a potential that the coin cell battery used to monitor X-Ray tube temperature may deplete early causing the system to become inoperable.

FDAJun 10, 2021Nationwide• GE OEC Medical Systems, Inc

Xolair Injection (Genentech) – Stability Specification (2021)

Failed Stability Specifications: Out of Specification results of Polysorbate 20 (PS20) content were detected at the 12 month testing time point.

Class IIModerate

FDAJun 9, 2021Nationwide• Genentech Inc

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation (Radiation Treatment Planning System) : RaySta...

Initial delivery positions will be set incorrectly when having setup beam(s) at the localization point.

FDAJun 8, 2021TN• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

GE Healthcare, LLC: SIGNA PET/MR, Tomographic Imager Combining Emission Compu...

GE Healthcare has recently become aware of an issue on the affected products listed below where the "Patient Orientation" button may inadvertently be clicked when intending to click on the "Save RX" button. This changes the prescribed patient orientation on the system prior to running the initial 3-Plane Localizer Scan (See Figure 1 for reference to buttons.) Selecting and saving a patient orientation that does not match the patient's actual position may result in incorrectly annotated and/or flipped images.

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: SIGNA Pioneer - Product Usage: is a whole body magnetic r...

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: SIGNA Creator, SIGNA Explorer, Nuclear Magnetic Resonance...

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

Eight Medical International BV Laan Van Hildernisse-Noord 2a Bergen Op Zoom Netherlands: Recirculator 8.0s Disposable Lavage Kit (product code num...

The patient may be exposed to potential aluminum ion release during warming therapy under certain use conditions.

FDAJun 4, 2021Nationwide• Eight Medical International BV Laan Van Hildernisse-Noord 2a Bergen Op Zoom Netherlands

GE Healthcare, LLC: SIGNA MR355, SIGNA MR360, Nuclear Magnetic Resonance Imag...

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: Discovery MR750 3.0T - Product Usage: is a whole body mag...

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: Optima MR450w 1.5T, Nuclear Magnetic Resonance Imaging Sy...

FDAJun 4, 2021Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: Discovery MR750w 3.0T - Product Usage: is a whole body ma...

FDAJun 4, 2021Nationwide• GE Healthcare, LLC