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. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 25301–25320 of 52,000 recalls
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 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: 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: 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 200-005-152 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 210-105-251 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 Natura Model 210-005-152 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 GENILook Model 200-005-153 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 200-105-151 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 200-005-151 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 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: 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.