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. 2,368 recalls have been distributed to Rhode Island in the last 12 months.
Showing 23181–23200 of 27,456 recalls
Recalled Item: Stryker 5.0mm Round Fluted Bur Aggressive Sterile Product Usage: The...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 3.0mm x 3.8mm Precision Neuro Drill Sterile Product Usage: Recalled...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 2.0mm Tapered Round Elite Bur Sterile Product Usage: The Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.0mm Egg Bur Sterile Product Usage: The devices are Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.5mm Round Fluted Bur Aggressive Sterile Product Usage: The...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 3.0mm Round Fluted Bur Soft Touch Sterile Product Usage: Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 6.0mm Round Fluted Bur Sterile Product Usage: The devices Recalled...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.0mm Barrel Bur Sterile Recalled by Stryker Instruments Div. of...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.0mm Zyphr Elite Round Fluted Bur Sterile Product Usage: Recalled...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vision Troubleshooting Guide for the da Vinci Standard Surgical System...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endowrist Instrument and Accessory Manual for the da Vinci Standard Recalled...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insert for IRK for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stapler Addendum for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vessel Sealer Addendum for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6000 analyzer series Operators Manual Roche cobas Recalled by Roche...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connection QRG for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Manual for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRK QRG for the da Vinci Standard Surgical System Recalled by Intuitive...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is Recalled by Brainlab AG...
The Issue: Brainlab Navigation Software Spine & Trauma 3D 2.0/2.1 offers automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System...
The Issue: A portion of the BBL Crystal Enteric/Nonfermentor (E/NF) Identification kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.