Medical DeviceJul 9, 2025
Philips VL13-5 Transducer recall — FDA Z-2063-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
21,924medical device recall records
2,160FDA Class I records
8firms with 5+ records
MEDLINE INDUSTRIES, LP…730 records
Database records
Records — page 128
21,924 detailed records are currently available in this category.
Medical DeviceJul 9, 2025
Philips L8-4 Transducer recall — FDA Z-2056-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
C.R. Bard BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr recall — FDA Z-2075-2025
Cather packaging may contain the incorrect French size.
Class IIFDA: OngoingC.R. Bard Inc.
Medical DeviceJul 9, 2025
Maquet Critical Care AB Servo-u MR Ventilator System recall — FDA Z-2015-2025
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active…
Class IFDA: OngoingMaquet Critical Care AB
Medical DeviceJul 9, 2025
Siemens Medical Solutions USA ARTIS is a family of dedicated angiography systems developed recall — FDA Z-2019-2025
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceJul 9, 2025
VITROS 4600 Chemistry System recall — FDA Z-2040-2025
a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Philips L9-3 Transducer recall — FDA Z-2057-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 recall — FDA Z-2045-2025
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 9, 2025
VITROS 5600 Integrated System recall — FDA Z-2038-2025
A software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Geneoscopy ColoSense Test Kit, Part No. 80-001, component of ColoSense test recall — FDA Z-2077-2025
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.
Class IIFDA: OngoingGeneoscopy, Inc.
Medical DeviceJul 9, 2025
Philips S7-3t Transducer recall — FDA Z-2060-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Siemens Healthcare Diagnostics ADVIA 120/2120/2120i SETpoint Calibrator recall — FDA Z-2086-2025
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJul 2, 2025
Becton Dickinson Infusion Therapy Systems REF: 381434 BD Insyte Autoguard Shielded IV recall — FDA Z-2007-2025
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class IIFDA: OngoingBecton Dickinson Infusion Therapy Systems, Inc.
Medical DeviceJul 2, 2025
Becton Dickinson Infusion Therapy Systems REF: 381923 BD Insyte Autoguard Winged Shielded IV recall — FDA Z-2006-2025
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class IIFDA: OngoingBecton Dickinson Infusion Therapy Systems, Inc.
Medical DeviceJul 2, 2025
GE Medical Systems China Co GE Healthcare LOGIQ F R3 Ultrasound System, Model/Catalog Number recall — FDA Z-2029-2025
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…
Class IIFDA: OngoingGE Medical Systems China Co., Ltd.
Medical DeviceJul 2, 2025
Philips Spectral CT. Computed tomography X-ray system recall — FDA Z-2034-2025
Devices with affected software may experience two unintended motion issues that may lead to contact between the Gantry or table with the operator or patient, along with additional software…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceJul 2, 2025
ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm recall — FDA Z-2008-2025
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 2, 2025
ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm recall — FDA Z-2011-2025
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 2, 2025
Becton Dickinson Infusion Therapy Systems REF: 382544 BD Insyte Autoguard Shielded IV recall — FDA Z-2005-2025
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class IIFDA: OngoingBecton Dickinson Infusion Therapy Systems, Inc.
Medical DeviceJul 2, 2025
Becton Dickinson & Co BD BACTEC MGIT 960 PZA Kit recall — FDA Z-2023-2025
BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates.
Class IIFDA: OngoingBecton Dickinson & Co.
Medical DeviceJul 2, 2025
Becton Dickinson Infusion Therapy Systems REF: 381433, BD Insyte Autoguard Shielded IV recall — FDA Z-2002-2025
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class IIFDA: OngoingBecton Dickinson Infusion Therapy Systems, Inc.
Medical DeviceJul 2, 2025
Terumo Cardiovascular Systems CDI OneView System BPM Probe: Cat recall — FDA Z-2018-2025
Due to an error in assembly of the thermistor within some units, the affected probes will experience inaccuracy in measured shunt sensor temperature. Additionally, following changes in…
Class IIFDA: OngoingTerumo Cardiovascular Systems Corporation
Medical DeviceJul 2, 2025
Becton Dickinson Infusion Therapy Systems REF: 381423, BD Insyte Autoguard, Shielded IV recall — FDA Z-1999-2025
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Class IIFDA: OngoingBecton Dickinson Infusion Therapy Systems, Inc.
Medical DeviceJul 2, 2025
Limacorporate S.p.A PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile recall — FDA Z-2025-2025
There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
Class IIFDA: OngoingLimacorporate S.p.A
How to use this medical device recall index
Medical device recall records can change as the FDA receives additional information. Check the official record identifier and current FDA information before making health or product-use decisions.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
What the database can and cannot tell you
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.