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 20841–20860 of 27,456 recalls
Recalled Item: Carto 3 EP Navigation System. Electro physiology system which views Recalled...
The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 3.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICroSTREP plus 1 Panel Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICroSTREP plus 2 Panel Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 8.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software Anomaly...
The Issue: Software Anomaly during ADD Installation on VITROS 5,1 FS Chemistry Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac...
The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kits used with the da Vinci Si Recalled by...
The Issue: B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for...
The Issue: Incorrect tubing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120)...
The Issue: DePuy Orthopaedics, Inc. is initiating a voluntary recall of select lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled by...
The Issue: The Inserter Inner Shaft would not fit through the Inserter. The inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...
The Issue: Complaints that the femoral head could not be assembled with its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...
The Issue: This product was produced using a finishing process not identified as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...
The Issue: There is a defect in one lot of a buffer, non-specific background staining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...
The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....
The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.