workplace Recalls

158 recalls tagged with “workplace”.

Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies uMI 550 MD PET/CT Recalled for 95 Units Over Mechanical Interference Risk (2025)

UIH Technologies LLC recalled 95 uMI 550 MD PET/CT systems sold in the United States after reports that third-party outer covers can become trapped between the patient table and gantry. The covers can interfere with table movement during imaging. Hospitals and clinics should stop using the devices and follow the manufacturer's recall instructions immediately.

UIH Technologies
Third-party outer
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus EVIS EXERA III BF-1TH190 Bronchoscope Recall 8,587 Units in 2025

Olympus Corporation of the Americas recalls 8,587 bronchovideoscope units worldwide, including 4,297 in the US and 4,290 outside. The recall centers on updated IFU language for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. Stop using the device immediately and follow manufacturer instructions for remediation.

Olympus Corporation of the Americas
Additional IFU
Read more
Health & Personal Care
HIGH
FDA DEVICE

MedicalCommunications GmbH Recalls 474 Ashvins HEYEX 2 / HEYEX PACS Software Units (2025)

MedicalCommunications GmbH recalled 474 Ashvins HEYEX 2 / HEYEX PACS software units distributed nationwide in the United States. The affected software versions range from 2.6.0 (Build 2088) to 2.6.8 (Build 2220). The hazard is that the measured value may be smaller than the actual area, potentially affecting imaging measurements. Stop using the software immediately and follow manufacturer recall‑s

MedicalCommunications
Potential that
Read more
Health & Personal Care
HIGH
FDA DEVICE

Draeger Atlan A350 Anesthesia Workstations Recalled for Ventilator Failures in 2025

Drӕager recalled 530 Atlan A350 anesthesia workstations imported from Draegerwerk AG and Co. KGaA and distributed to 25 U.S. states and more than 30 countries. The device can experience a piston ventilator failure before use or fail to ventilate during use. Hospitals should stop using affected units immediately and follow Draeger recall instructions.

Draeger
The device
Read more
Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare CSCS V3 MAS800 Central Station Recalled for 2,306 Units Worldwide (2025)

GE Healthcare recalled 2,306 CSCS V3 MAS800 Central Station desktops worldwide after identifying a software fault that can trigger a continuous reboot cycle. The issue can result in a loss of central monitoring for connected patients. Hospitals should stop using the affected devices and follow the recall instructions from GE HealthCare and Wipro GE Healthcare Private Ltd.

GE Healthcare
GE HealthCare
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound C9-4 Transducer Recalled for Lifespan Labelling — 1 Unit (2025)

Philips Ultrasound recalled 1 unit of the C9-4 Ultrasound Transducer, Model No. 989605365021, distributed nationwide in the United States. The recall focuses on clarifying and labeling the device’s useful life. Healthcare providers and patients should stop using the device immediately and follow Philips’ instructions for replacement or further steps.

Philips Ultrasound
To provide
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)

Philips Ultrasound recalled 2 units of the Philips OMNI II TEE Ultrasound Transducer sold nationwide through multiple retailers. The recall seeks labeling clarification to define the transducer's useful life. Healthcare facilities should stop using the devices and follow Philips recall instructions.

Philips Ultrasound
To provide
Read more
Health & Personal Care
HIGH
FDA DEVICE

Lutronic XERF EFFECTOR 60 Electrosurgical Unit Recalled for Manufacturing Defects (2025-2026 Models)

Lutronic recalled 7,490 XERF EFFECTOR 60 electrosurgical units distributed worldwide, including several U.S. states, after manufacturing defects surfaced between April 1 and August 20, 2025. The defect can cause adverse events for patients. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.

Lutronic
Manufacturing defects
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland Recall Expands for Allura Xper FD20/15 OR Table Model 722059 (2025

Philips Medical Systems Nederland B.V. recalls 8 medical tables worldwide due to BIOS battery depletion risk. The recall affects Allura Xper FD20/15 OR Tables with model number 722059. The BIOS battery may deplete faster than expected, causing the system not to start without warning. Hospitals and healthcare providers should stop using the device immediately and follow the recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems FD20 Biplane OR Table Recall for BIOS Battery Depletion (2025)

Philips Medical Systems Nederland B.V. recalls Allura Xper FD20 Biplane OR Table models 722020 and 722025. Four units are affected worldwide, including two in the United States. The BIOS battery may deplete faster than expected, halting the system startup with no user warning. The recall advises stop-use and coordination with healthcare providers for instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Read more
Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter Recall 173 Un­

Northeast Scientific recalled 173 units of the NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter distributed nationwide to U.S. healthcare facilities. The device is not cleared for marketing in the United States due to sterility concerns. A breach in the sterile barrier packaging could compromise sterility. Health care providers and patients should stop using the device immediately.

Northeast Scientific
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Vida MRI Recall 237 Units Worldwide Over Ice Blockage Risk (2025)

Siemens Medical Solutions USA recalled 237 MAGNETOM Vida MRI scanners sold worldwide to healthcare providers. The recall cites ice forming in the magnet venting system. A quench could lead to a helium leak into the scanning room. Hospitals must stop using the devices and await manufacturer instructions.

Siemens Medical Solutions USA
There is
Read more
Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Verio Dot MRI Recall 30 Units Over Ice Blockage Risk (2025)

Siemens Medical Solutions USA recalled 30 MAGNETOM Verio Dot MRI systems sold worldwide through hospitals and medical facilities. The ice blockage in the magnet venting system could trap helium during a quench, causing pressure buildup and a potential helium leak into the scanning room. Facilities should stop using the devices immediately and follow the manufacturer’s recall instructions.

Siemens Medical Solutions USA
There is
Read more
Health & Personal Care
HIGH
FDA DEVICE

Frontier Devices Recalls 2,700 REF 301.914S1 14 mm Distraction Pins (2025)

Frontier Devices recalled 2,700 units of REF 301.914S1 14 mm Distraction Pin sold nationwide by multiple retailers. The labeling includes shelf life that has not been validated. Healthcare providers and patients should stop using this device immediately and follow the manufacturer’s recall instructions.

Frontier Devices
Labeling includes
Read more
Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recalled for Safety Architecture Software Issue (41,009 Units, 2025)

Boston Scientific recalled 41,009 pacemakers worldwide after a software flaw could prevent Safety Mode activation. The defect affects devices in the ACCOLADE family and several related models. Patients and healthcare providers should stop using the device immediately and follow recall instructions from the manufacturer.

Boston Scientific
Software to
Read more
Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Heartstring III Proximal Seal System Recalled for 168 Units Worldwide (2025)

Maquet Cardiovascular recalled 168 Heartstring III Proximal Seal System intravascular occluders worldwide, including the United States. Three failure modes have been identified: loading the Heartstring Seal, deploying it into the aortotomy, and achieving adequate hemostasis. Healthcare facilities should stop using the device and follow the manufacturer’s recall instructions.

Maquet Cardiovascular
Three failure
Read more
Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter UniCel DxH 690T Hematology Analyzer Recall Over HGB Photometer (2025)

Beckman Coulter recalled the UniCel DxH 690T COULTER Cellular Analysis System configured with the LED HGB Photometer REF C34520. The hematology analyzer may produce erroneously high hemoglobin results on samples with elevated white blood cell counts. Labs should stop using the device immediately and follow Beckman Coulter's recall instructions.

Beckman Coulter
Hematology analyzers
Read more
Previous
12345...8
Next

Tag Statistics

Total Recalls
158

Related Tags

electronicfda regulatedcpsc regulatedimmediate actionstop use immediatelyreplacement availablereturn for refundkitchenmetalplasticadult productinfant product