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 15481–15500 of 29,188 recalls
Recalled Item: Genicon Natura Model 210-005-051 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon Natura Model 210-005-251 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon Natura Model 210-005-151 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-005-251 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-105-252 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-105-251 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon GENILook Model 200-105-152 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon Natura Model 210-005-052 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to The...
The Issue: The catheter failed the endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitalBeam Radiotherapy Delivery System Version 2.5 Product Usage: The...
The Issue: Reports have been received of an anomaly that can result in a treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy...
The Issue: Reports have been received of an anomaly that can result in a treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA Circular Stapler with Tri-Staple Technology Recalled by COVIDIEN LLC Due...
The Issue: The firm identified the potential for a device to have an incorrect tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DxTerity(TM) TRA 5F Recalled by Medtronic Vascular Due to...
The Issue: Medtronic has determined that the French size indicator on the inner pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Olecranon Hook Plate Recalled by TriMed Inc. Due to The firm has...
The Issue: The firm has become aware that the angled-hole of certain semi-tubular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.