Class IIOngoingZ-1561-2025
Straumann USA LLC recalls TLX/TLC SP Guided Implant Driver
The devices are missing the laser marked depth markings.
Straumann USA LLCMAApr 23, 2025
2025 device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 2,053–2,064 of 2,908 recalls
Class IIOngoingZ-1560-2025
Baxter Healthcare Corporation recalls Welch Allyn CP150 Electrocardiograph:
There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
Baxter Healthcare Corp…ILApr 23, 2025
Class IIOngoingZ-1559-2025
Baxter Healthcare Corporation recalls Welch Allyn CONNEX Accessory Power Management Stand:
There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
Baxter Healthcare Corp…ILApr 23, 2025
Class IIOngoingZ-1558-2025
Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor (CVSM):
There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
Baxter Healthcare Corp…ILApr 23, 2025
Class IIOngoingZ-1557-2025
Abbott Medical recalls Aveir DR Leadless Pacemaker (LP) Ventricular Device REF LSP202V UDI-DI code: 05415067…
Due to a manufacturing issue, leadless pacemakers may have been exposed to higher than normal temperatures which may result in premature battery failure.
Abbott MedicalCAApr 23, 2025
Class IIOngoingZ-1556-2025
GE Medical Systems, LLC recalls Venue Fit Models: R3 (Model Number H45303VFSC
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
GE Medical Systems, LL…WIApr 23, 2025
Class IIOngoingZ-1555-2025
GE Medical Systems, LLC recalls Venue Go Models: R2 (Model Number H45181VG)
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
GE Medical Systems, LL…WIApr 23, 2025
Class IIOngoingZ-1554-2025
Philips North America LLC recalls Philips DXR System
Potential for collimator to fall as a result of incorrect installation.
Philips North America…MAApr 23, 2025
Class IIOngoingZ-1553-2025
Philips North America LLC recalls Philips DXR System
Potential for collimator to fall as a result of incorrect installation.
Philips North America…MAApr 23, 2025
Class IIOngoingZ-1552-2025
CareFusion 303, Inc. recalls MEDFLEX
If "Clear All" selected medications is selected on patient profile, the automated dispensing cabinet may allow dispensing of medication without first requiring the RxVerify Validation Code be entered/without validation f…
CareFusion 303, Inc.CAApr 23, 2025
Class IOngoingZ-1533-2025
ZOLL Circulation, Inc. recalls Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform M…
AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
ZOLL Circulation, Inc.CAApr 23, 2025
Class IOngoingZ-1528-2025
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 2271…
Lack of sterility assurance for closed suction catheter systems
Avanos Medical, Inc.GAApr 23, 2025