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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 241–260 of 1,000 recalls

Class IIOngoing

Brand Name: VERIQA; Product Name: RT MonteCarlo 3D v3; Model/Catalog Number: S070031.520; Software Version: 3.1.18;

PTW FREIBURG

When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorrectly omit the bolus during treatment and deliver the prescribed dose to the wrong tissue depth.

August 4, 2026 · DeviceView details →
Class IIOngoing

Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025

B Braun Medical Inc

Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.

August 4, 2026 · DeviceView details →
Class IIOngoing

Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 / 14987666542965 B96693 / 14987666542972 B12183 / 14987666540671 The AU480 Chemistry Analyzer measure analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC) material, and other accessories. This system is for in vitro diagnostic use only.

Beckman Coulter Mishima K.K.

Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError AlarmDB when launching the instrument software, using PC pre-installed with Microsoft SQL Server 2022 Express. When this occurs, AlarmDB becomes unreadable and the instrument software cannot be started. This causes a delay in obtaining patient results.

August 3, 2026 · DeviceView details →
Class IIOngoing

Brand Name: VOLARA System Product Name: VOLARA, HC, NA A Model/Catalog Number: M08594A Software Version: N/A Product Description: VOLARA, HOMECARE, NORTH AMERICA Component: No

Baxter Healthcare Corporation

Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to firm and testing confirmed devices meet specifications.

August 3, 2026 · DeviceView details →
Class IIOngoing

HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF: 10301012 (EU); HEALON DUET PRO II, REF: 10301016 (EU)

Johnson & Johnson Surgical Vision, Inc.

Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during insertion, withdraw cannula and reassess the insertion conditions (i.e. insertion angle, incision size, etc.) before proceeding because forcing the cannula may cause corneal abrasion, iris trauma or descemet's membrane detachment.

July 31, 2026 · DeviceView details →
Class IIOngoing

Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions

GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

July 31, 2026 · DeviceView details →
Class IIOngoing

Philips PIC iX Essentials REF:867093

Philips North America

Due to software malfunction, patient information system may freeze and become unresponsive.

July 31, 2026 · DeviceView details →
Class IIOngoing

New York Embroidery Studio Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large. Model Number: NYES100-2. Packaged in inner packs of 10 and 100 gowns per shipping case.

New York Embroidery Studio, Inc.

Gowns do not consistently meet the minimum liquid-barrier performance required.

July 31, 2026 · DeviceView details →
Class IIOngoing

Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution, printing, editing, and processing of digital images and data acquired from diagnostic imaging devices, All versions

GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

July 31, 2026 · DeviceView details →
Class IIOngoing

MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;

Bayer Medical Care, Inc.

Some devices may not have been properly sterilized due to a manufacturing sterilization issue.

July 31, 2026 · DeviceView details →
Class IIOngoing

Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS);

Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

July 31, 2026 · DeviceView details →
Class IIOngoing

Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions

GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

July 31, 2026 · DeviceView details →
Class IIOngoing

Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS);

Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

July 31, 2026 · DeviceView details →
Class IIOngoing

Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A

Medline Industries, LP

Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

July 31, 2026 · DeviceView details →
Class IIOngoing

Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A

Medline Industries, LP

Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

July 31, 2026 · DeviceView details →
Class IIOngoing

Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise imaging workflows, All versions

GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

July 31, 2026 · DeviceView details →
Class IIOngoing

SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25

WELL LEAD MEDICAL CO. LTD

The 6Fr suction catheter could not pass through the samples smoothly.

July 31, 2026 · DeviceView details →
Class IIOngoing

Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applications, All versions

GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

July 31, 2026 · DeviceView details →
Class IIOngoing

Philips Patient Information Center iX REF:866389

Philips North America

Due to software malfunction, patient information system may freeze and become unresponsive.

July 31, 2026 · DeviceView details →
Class IIOngoing

Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions

GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

July 31, 2026 · DeviceView details →
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