Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,928 recalls have been distributed to Ohio in the last 12 months.
Showing 25481–25500 of 30,087 recalls
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 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 1.3mm Wire Pass Drill Sterile Product Usage: The devices 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: Lindemann Drill Short Recalled by Stryker Instruments Div. of Stryker...
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 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 0.5mm 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 6.0mm Acorn 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: 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: 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.
Recalled Item: RUSCH Easy Cath Coude Kit Recalled by Teleflex Medical Due to Product was...
The Issue: Product was packaged with a straight catheter rather than the correct coude...
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: 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: Integra UCR 3mm Hex Recalled by SeaSpine Inc Due to Integra has identified...
The Issue: Integra has identified through an investigation of complaints that there may...
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: 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: 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: Natural Rubber Latex QRG for the da Vinci Standard Surgical System 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: Single Site US Manuals and Single Site OUS Manuals for 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.