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. 2,603 recalls have been distributed to Tennessee in the last 12 months.
Showing 17181–17200 of 29,188 recalls
Recalled Item: Health Harmony Mobile application software Product Usage: Care Innovations...
The Issue: It was discovered that in certain situations, including partial sessions and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to An accessory...
The Issue: An accessory (range shifter, ridge filter&) can be improperly inserted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the Recalled by...
The Issue: A software malfunction was found where WBC, RBC and PLT comments added after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power PORT-A-CATH II Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...
The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volumat MC Agilia Volumetric Infusion Pump Recalled by Fresenius Vial Sa Due...
The Issue: Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sundream 12 V tanning bed Recalled by ProSun International, LLC Due to The...
The Issue: The 30 minute maximum tanning time has been reduced to 20 minutes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Module 3 monitoring spirometer Recalled by Mindray DS USA, Inc. dba...
The Issue: The firm made multiple changes to the product requiring the submission of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEKTA Digital Accelerator under the following brand names: Elekta Synergy...
The Issue: There is a potential for an uncontrolled extension of iViewGT / XVI detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating IV Pole Rotating IV Pole falls under the category Recalled by...
The Issue: There is the potential for the Rotating IV Pole to fall. A fall could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.