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. 2,636 recalls have been distributed to Tennessee in the last 12 months.
Showing 15361–15380 of 29,188 recalls
Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...
The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...
The Issue: Cross contamination may have occurred between wells for the reagent pack. As...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...
The Issue: Software Update: External USB Drive performance and its impact on Graphic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK Recalled...
The Issue: One lot of the Legion AP femoral cutting block, size 6, was manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...
The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...
The Issue: The power supply unit for the printer used with the device can potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...
The Issue: Data loggers showed that one shipment to the United States experienced low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...
The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ E10 Ultrasound System Recalled by GE Healthcare, LLC Due to There...
The Issue: There is a potential for an undetected over temperature condition on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium MC Recalled by GE Healthcare, LLC Due to A detector...
The Issue: A detector can detach and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma...
The Issue: A detector can detach and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...
The Issue: Potential to lead to a false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH...
The Issue: A detector can detach and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled...
The Issue: The pouches of certain lots of product may have wrinkles along the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled by...
The Issue: The pouches of certain lots of product may have wrinkles along the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...
The Issue: The pouches of certain lots of product may have wrinkles along the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...
The Issue: The pouches of certain lots of product may have wrinkles along the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock...
The Issue: There is potential to break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek¿ XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips...
The Issue: Abnormally high INR test results with the affected CoaguChek test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System Recalled...
The Issue: The service manual was not updated at the time of the release of software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.