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  1. FDA Recalls
  2. ›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 721–740 of 1,000 recalls

Class ITerminated

Vitek 2 Gram Positive Susceptibility Test Cards (AST-P643 REF 418671), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.

Biomerieux Inc

Product insert fails to identify performance limitation related to EUCAST breakpoints for Teicolplanin.

February 24, 2016 · DeviceView details →
Class ITerminated

Dexcom G4 PLATINUM (Professional) Receiver Receiver Part Number: MT20649 Receiver (mg/dL), Black. Intended to detect trends and track glucose patterns in persons with diabetes. The G4 PLATINUM CGM System and G4 PLATINUM (Professional) CGM System use the same receiver, MT20649. The kits differ due to other kit contents, such as indications for use and professional receiver shield.

Dexcom Inc

Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.

February 23, 2016 · DeviceView details →
Class ITerminated

Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430 Receiver (mg/dL), Black (pediatrics); MT22430-PNK, Receiver (mg/dL), Pink (pediatrics); MT22430-BLU, Receiver (mg/dL); Blue (pediatrics). Intended to detect trends and track glucose patterns in persons with diabetes.

Dexcom Inc

Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.

February 23, 2016 · DeviceView details →
Class ITerminated

Dexcom G4 PLATINUM Receiver Receiver Part Number: MT20649 Receiver (mg/dL), Black; MT20649-PNK, Receiver (mg/dL), Pink; MT20649-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.

Dexcom Inc

Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.

February 23, 2016 · DeviceView details →
Class ITerminated

Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL), Black; MT22719-PNK, Receiver (mg/dL), Pink; MT22719-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.

Dexcom Inc

Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.

February 23, 2016 · DeviceView details →
Class ITerminated

Dexcom G4 PLATINUM (Pediatric) Receiver with Share Receiver Part Number: MT22608 Receiver (mg/dL), Black (pediatrics); MT22608-PNK, Receiver (mg/dL), Pink (pediatrics); MT22608-BLU, Receiver (mg/dL), Blue (pediatrics). Intended to detect trends and track glucose patterns in persons with diabetes.

Dexcom Inc

Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.

February 23, 2016 · DeviceView details →
Class ITerminated

Dexcom G4 PLATINUM Receiver with Share Receiver Part Number: MT22495 Receiver (mg/dL), Black; MT22495-PNK, Receiver (mg/dL), Pink; MT22495-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.

Dexcom Inc

Customers may not receive an intended audible alarm or alert if relying on hearing the alarm or alert.

February 23, 2016 · DeviceView details →
Class ITerminated

Percutaneous Insertion Tray; Product Code: IAK-06845 The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

Ultra 8 IAB: 8Fr 30cc; Product Code: IAB-05830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

UltraFlex IAB: 7.5Fr 30cc; Product Code: IAB-06830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

UltraFlex IAB: 7.5Fr 40cc; Product Code: IAB-06840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

Percutaneous Insertion Tray; Product Code: IAK-S7IT The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2850, MOL1451, MOL1452, MOL1455

Focus Diagnostics Inc

Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied with the Simplexa HSV 1 & 2 Direct (MOL2150), Simplexa Flu A/B & RSV Direct (MOL2650) and Simplexa Group A Strep Direct kits (MOL2850) because it may result in a false negative result, a false positive result or Error code (s) 500 or 505, and it may result in higher invalid rates.

February 10, 2016 · DeviceView details →
Class ITerminated

Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2150, MOL1451, MOL1452, MOL1455

Focus Diagnostics Inc

Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied with the Simplexa HSV 1 & 2 Direct (MOL2150), Simplexa Flu A/B & RSV Direct (MOL2650) and Simplexa Group A Strep Direct kits (MOL2850) because it may result in a false negative result, a false positive result or Error code (s) 500 or 505, and it may result in higher invalid rates.

February 10, 2016 · DeviceView details →
Class ITerminated

FiberOptix Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-LWS The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.

Arrow International, Inc., Division of Teleflex Medical Inc.

The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.

February 10, 2016 · DeviceView details →
Class ITerminated

MitraClip Clip Delivery System, product number MSK0101. The MitraClip System contains the Clip Delivery System, product number CDS0201, GTIN 08717648195914 and the Steerable Guide Catheter, product number SGC0101, GTIN 08717648195921. The MitraClip Clip Delivery System (CDS) consists of three major components: 1) the Delivery Catheter 2) the Steerable Sleeve, and 3) the MitraClip device. The implantable MitraClip device is located at the distal end of the CDS. The CDS is used to advance and manipulate the implantable MitraClip device for proper positioning and placement on the mitral valve leaflets. The Delivery Catheter, which is part of the CDS, is designed to deliver and deploy the MitraClip. The Delivery Catheter extends through the thru-lumen of the Steerable Sleeve.

Abbott Vascular

Abbott Vascular has recently received reports of cases on Clip Delivery System devices that contain the One-Way Actuator Knob where a user attempted implanting a MitraClip, but the Clip could not be detached from the delivery system due to a mandrel fracture.

February 4, 2016 · DeviceView details →
Class ITerminated

Evita Infinity V500 Ventilator; Babylog Infinity VN500 Ventilator. Ventilation.

Draeger Medical, Inc.

The battery capacity of the optional PS500 power supply unit for the Infinity (ACS) Workstation Critical and Neonatal Care was rapidly and unexpectedly reduced, despite using the most recent power supply firmware version 1.50 released in November 2015 (recall Z-0436-2016). The batteries were prematurely discharged, even though an adequate battery charge status was displayed on the device.

February 4, 2016 · DeviceView details →
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