Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22181–22200 of 29,188 recalls
Recalled Item: One Step Button Recalled by Boston Scientific Corp Due to Boston Scientific...
The Issue: Boston Scientific Corp. initiated a voluntary recall of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJ-1606 Instrument Channel Adaptor Recalled by Olympus Corporation of the...
The Issue: small puncture marks in a sterile package for an accessory to an Olympus device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NicoletOne Software v5.94 Recalled by Natus Neurology Inc Due to When using...
The Issue: When using the NicoletOne v5.94 software, after exiting the impedance check...
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: 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 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: 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: 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: 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: 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: 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 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: 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: 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: 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 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: 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: 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.