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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 3241–3260 of 39,430 recalls

Class IIOngoing

REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOnly

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IIOngoing

REF: 382544 BD Insyte Autoguard Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IIOngoing

REF: 381433, BD Insyte Autoguard Shielded IV Catheter, 20GA x 1.00 in (1.1x25 mm) 65 mL/min, STERILEEO, RxOnly

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IIOngoing

STA - Owren Koller. Model/Catalog Number: 00360 STA - Owren-Koller is a buffer solution intended for use as a diluent for reagents and human plasmas in coagulation tests performed with analyzers of the STA-R, STA Compact, STA Satellite and ST art families.

Diagnostica Stago, Inc.

Potential for shorter clotting times in clotting tests which have a dilution, leading to possible overestimate of around 1%

May 21, 2025 · DeviceView details →
Class IIOngoing

REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IIOngoing

REF: 382944, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IIOngoing

REF: 381533, BD Insyte Autoguard Winged, Shielded IV Catheter, 20 GA x 1.00 in (1.1 x 25 mm) 65mL/min, STERILEEO,RxOnly

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IOngoing

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU, HT70M-WW-NA, HT70-SY-EU. Newport HT70Plus Ventilator, REF: HT70PM-ES-EU, HT70PM-ES-NA, HT70PM-JP-NA, HT70PM-PT-BR, HT70PM-SY-AS, DLHT70PM-WW-NA, HT70PM-SY-NA, HT70PM-SY-UK, HT70PM-WW-EU, HT70PM-WW-UK, HT70PM-SY-EU, HT70PM-WWNA. HT70-2 CONTROL BOARD ROHS X1, REF: GR105796. HT70P CONTROL BOARD ROHS X1, REF: GR105795. HT70 Conversion Kit, REF: GRFSKHT70M-2.

Covidien

Ventilator Printed Circuit Board Assembly may have two separate capacitors that may fail, which may result in the ventilator either shutting down during use, thus necessitating use of an alternate form of ventilation, or the shutdown alert alarm fails to alarm effectively during shut down, which may result in respiratory failure, hypoventilation, low oxygen saturation, hypoxia, treatment delay.

May 21, 2025 · DeviceView details →
Class IIOngoing

REF: 381811, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IIOngoing

Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release Configuration, Rev H SW-300689-02 Bigfoot Inject v1 Pen Cap RCAP Firmware 1.3.0 Release Configuration, Rev H The Bigfoot Unity Diabetes Management System that include the Pen Caps (Rapid-Acting Insulin Pen Cap [RCAP] and Long-Acting Insulin Pen Cap [LCAP]) integrates continuous monitoring with insulin dose recommendations. The Pen Caps (Rapid-Acting Insulin Pen Cap [RCAP] and Long-Acting Insulin Pen Cap [LCAP]) are part of the Bigfoot Unity Diabetes Management System.

BIGFOOT BIOMEDICAL

Due to a software/firmware issue diabetes management system may provide a device error and cause the insulin pen to become unresponsive and unable to function. This error may pose a potential health risk for people living with diabetes as they may not have all information necessary to make a timely treatment decision.

May 21, 2025 · DeviceView details →
Class IIOngoing

LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.

Jolife AB

Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.

May 21, 2025 · DeviceView details →
Class IIOngoing

REF: 382633, BD Insyte Autoguard BC Winged, Shielded IV Catheter with Blood Control Technology, 20GA x 1.00 in (1.1x25 mm) 63 mL/min, STERILEEO, RxOnly

Becton Dickinson Infusion Therapy Systems, Inc.

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

May 21, 2025 · DeviceView details →
Class IIOngoing

BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).

Becton Dickinson & Co.

BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates.

May 20, 2025 · DeviceView details →
Class IIOngoing

My3D Personalized Solutions Humeral Cup, Model Number: C24-0223-0003. It is a component of a Custom Constrained Shoulder Arthroplasty Device

Onkos Surgical, Inc.

Required inspections were not performed on finished product prior to release and distribution.

May 20, 2025 · DeviceView details →
Class IIOngoing

ColoSense Test Kit, Part No. 80-001, component of ColoSense test

Geneoscopy, Inc.

Multiple plate failures documented as a result of the Low Positive Template Control being too high and out of range using the affected lot of ColoSense Test Kit.

May 20, 2025 · DeviceView details →
Class IIOngoing

PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile

Limacorporate S.p.A

There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.

May 19, 2025 · DeviceView details →
Class IIOngoing

PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile

Limacorporate S.p.A

There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.

May 19, 2025 · DeviceView details →
Class IIOngoing

Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Catalog Number: REF I-D-BMF90, 1 Single-Use Bipolar Minifork Stimulation Probe, 90mm, and 1 Green Ground Needle ; REF 1-D-BMF90-5, lot number 050925219, expiration 2028-11-30 I-D-BMF90-5 Stimulated EMG Kit with Hummingbird - Box of 5 Kits - Each Kit Includes: 1 Single-Use Bipolar Minifork Stimuation Probe, 90mm, and 1 Green Ground Needle

Neurovision Medical Products Inc

Product packaging contains the wrong part number and kit contents.

May 19, 2025 · DeviceView details →
Class IIOngoing

Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Description: The DRS Vascular Q-Stop Suture Retention Appliance is a sterile, single-use, lightweight device made of biocompatible materials that can be easily installed within minutes to assist with venous access hemostasis. Component: No

Drs Vascular, Inc

XXX

May 16, 2025 · DeviceView details →
Class IIOngoing

GE Healthcare LOGIQ F R3 Ultrasound System, Model/Catalog Number 5943263, diagnostic ultrasound system

GE Medical Systems China Co., Ltd.

GE HealthCare has become aware that the Estimated Fetal Weight (EFW) measurement data feature on the Versana Premier R3 and LOGIQ F R3 series ultrasound systems can display previous obstetric patient data in the Whizz report. This could potentially lead to an incorrect clinical decision due to inaccuracy in the fetal size and growth calculation.

May 16, 2025 · DeviceView details →
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