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. 1,988 recalls have been distributed to Tennessee in the last 12 months.
Showing 11641–11660 of 29,188 recalls
Recalled Item: Alaris System PC Unit Model 8000 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DCA Vantage Handheld Barcode Scanner - Zebra Model - Model Recalled by...
The Issue: If DCA Vantage Analyzer is configured to run Code 39 with check digit, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris SpO2 Module Model 8210 and Model 8220 Recalled by CareFusion 303,...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...
The Issue: Potential for sterile packaging to be compromised¿
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Auto ID Module Model 8600 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015. modular infusion pump and monitoring...
The Issue: If one or more screws or washers are loose or missing causing the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI-LOC TARGETER 4.5MM DISTAL FEMUR Recalled by Smith & Nephew, Inc. Due to...
The Issue: The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage:...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOSS DeBakey "Gator-Grip" Needle Holder 2 mm tip Recalled by Boss...
The Issue: The tungsten carbide plate, which is intended to hold the sewing needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVA Recalled by Precision Valve & Automation,Inc Due to While operating the...
The Issue: While operating the machine in "Run" mode an unexcepted event may occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InnoWave Sonic Irrigator Recalled by Steris Corporation Due to A recent FDA...
The Issue: A recent FDA inspection at the firm identified that the foil test performed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America, LLC...
The Issue: The device may experience an interruption of gas measurement due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite with software versions syngo.via VB30 or VB40...
The Issue: If the user modifies for any reason (e.g. reduction of artifacts) the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX ULTRA Suture Recalled by Smith & Nephew, Inc. Due to A packaging...
The Issue: A packaging error resulted in a XL drill being presented for use instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew T-F1X0 RCG Drill Pac Recalled by Smith & Nephew, Inc. Due to...
The Issue: The T-Fix sterile package contains only one sleeve instead of two, The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.