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Northwind Pharmaceuticals LLC

Northwind Pharmaceuticals LLC Recalls

All product recalls associated with Northwind Pharmaceuticals LLC.

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Recall Summary

Total Recalls

1000

Past Year

593

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 1801–1820 of 10391 recalls

BusPIRone Tablets (Northwind Pharmaceuticals) – Manufacturing Deviation (2023)

CGMP Deviations

Class IIModerate

FDAMar 16, 2023Nationwide• Northwind Pharmaceuticals LLC

Dianeal Low Calcium Dialysis Solution (Baxter Healthcare) – Sterility Concern (2023)

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Class IIModerate

FDAMar 15, 2023Nationwide• Baxter Healthcare Corporation

Dianeal PD-2 Dialysis Solution (Baxter Healthcare) – Sterility Concern (2023)

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Class II

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Moderate

FDAMar 15, 2023Nationwide• Baxter Healthcare Corporation

Hamilton-C6 Ventilator (Hamilton Medical) – safety ventilation error (2023)

Software error causes, safety ventilation, in which ventilation continues in the "safety ventilation" mode with audible/visible alarm - patient inputs are not monitored, if the following coincide 1) A mode change to an adaptive mode (ASV, APVcmv, APVsimv, INTELLiVENT-ASV, (S)CMV+, SIMV+), and 2) The controller and/or humidifier is connected to the ventilator and is operational.

FDAMar 14, 2023Nationwide• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Quantum Perfusion Systems (Spectrum Medical) – bobbin lock fault (2023)

The ratchet and pawl had an out of tolerance geometry which exhibited as the left bobbin would not lock.

FDAMar 13, 2023Nationwide• Spectrum Medical Ltd. Harrier 4, Meteor Business Park Cheltenham Road East Gloucester United Kingdom

DeVilbiss Healthcare Oxygen Concentrator (DeVilbiss) – Manual Update (2023)

The instruction manual is being replaced with an updated version that is in alignment with labeling requirements specified in the IEC-60101-1 standard.

FDAMar 9, 2023Nationwide• DeVilbiss Healthcare LLC

DigitalDiagnost C50 (Philips) – Spring Balancer Tension (2023)

If the PM for the telescopic carriage is not performed annually as defined in the Instructions for Use (IFU), the tension force of the spring balancer inside of the telescopic carriage will unavoidably decay through normal wear and tear; as a result there is a potential that the Ceiling Suspension of the DigitalDiagnost C50 system may descend inadvertently if power to the system is interrupted, and may result in injuries to patients and users

FDAMar 9, 2023Nationwide• Philips North America Llc

Jardiance 25mg Tablets (Boehringer) – Label Mix-up (2023)

Labeling: Label Mix-up

Class IIModerate

FDAMar 9, 2023Nationwide• Boehringer Ingelheim Pharmaceuticals, Inc.

DigitalDiagnost C50 (Philips) – Spring Balancer Tension (2023)

FDAMar 9, 2023Nationwide• Philips North America Llc

REX Pressure Therapy System (Compass Health) – User Manual Error (2023)

Error in the Introduction section of the user manual that indicates the device may be used for the prevention of deep vein thrombosis (DVT). Marketed without a 510k for this indication

FDAMar 7, 2023Nationwide• Compass Health Brands (Corporate Office)

EarlyVue VS30 Vitals Monitor (Philips) – CO2 Measurement Risk (2023)

EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing Calibration Alarm, a risk of an inaccurate CO2 measurement which may lead to a failure to recognize a change in patient condition.

FDAMar 6, 2023Nationwide• Philips North America Llc

EarlyVue VS30 Vitals Monitor (Philips) – CO2 Measurement Risk (2023)

FDAMar 6, 2023Nationwide• Philips North America Llc

CombiDiagnost R90 R1.1 (Philips) – Compliance Issue (2023)

Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0, CombiDiagnost R90 R.1.0 and CombiDiagnost R90 R1.1 systems are missing a certification label required by the Food and Drug Administration (FDA).

FDAMar 3, 2023Nationwide• Philips North America

ProxiDiagnost N90 R.1.0 (Philips) – Compliance Issue (2023)

FDAMar 3, 2023Nationwide• Philips North America

CombiDiagnost R90 R.1.0 (Philips) – Compliance Issue (2023)

FDAMar 3, 2023Nationwide• Philips North America

Multi-Purpose Kids Bike Helmets (Huizhou Lanova) - head injury risk (2023)

This recall involves Ouwoer Kids Bike Helmets with production date 202201. The helmets are red with black straps and a black buckle. The production date is printed on a white label on the inside of the helmet.

CPSCMar 2, 2023Nationwide• Huizhou Lanova Outdoor Product Company, of China

United Imaging PET System (Shanghai United Imaging) – Scatter Correction Failure (2023)

Due to a software issue where the process of patient scanning, the scatter correction may occasionally fail with will potentially cause a failure of the PET image reconstruction and generation of PET images.

FDAMar 1, 2023Nationwide• Shanghai United Imaging Healthcare Co., Ltd. No. 2258 Chengbei Rd, Jiading Ind. Shanghai China

FujiFilm FDR AQRO X-ray (FujiFilm) - Arm Breakage (2023)

Arm which holds the tube head in place is susceptible to breaking, if the device breaks it could potentially cause serious harm or injury to the patient and/or user.

FDAFeb 27, 2023Nationwide• FUJIFILM Healthcare Americas Corporation

Thor Motor Coach Hurricane (Thor) - Cabinet Mounting (2023)

Thor Motor Coach (TMC) is recalling certain 2018-2021 Hurricane and Windsport recreational vehicles. The driver and front passenger overhead cabinets may detach.

NHTSAFeb 24, 2023Nationwide• THOR MOTOR COACH

Artificial Eye Ointment (Global Pharma) – Bacterial Contamination (2023)

Non-Sterility: FDA analysis found unopened tubes to be contaminated with bacteria.

Class IHigh

FDAFeb 24, 2023Nationwide• Global Pharma Healthcare Private Limited