Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,390 recalls have been distributed to Rhode Island in the last 12 months.
Showing 20921–20940 of 27,456 recalls
Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...
The Issue: Cracks were discovered in the PET tray of a small population of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...
The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actifuse ABX/Actifuse MIS System A bone void filler intended only Recalled...
The Issue: Baxter Healthcare is issuing a voluntary recall for all lots of Actifuse ABX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....
The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...
The Issue: patient procedure interruption due to a potential system failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...
The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LX3 Floor Stand for Endure Luxite Envision Optical System Recalled by Alcon...
The Issue: Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...
The Issue: DLS pin breakage during planned implant removal, after uneventful and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: The Centricity...
The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: The Centricity Universal Viewer...
The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cadiere Forceps Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maryland Dissector Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crocodile Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fundus Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.