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 17321–17340 of 29,188 recalls
Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...
The Issue: Stent length on the label may not match the length of the stent itself.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...
The Issue: The firm received reports of two breakages of the pin tips which occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM0405 Mueller-Hinton Broth IVD Recalled by Remel Inc Due to Product may...
The Issue: Product may have incorrect cation information detailed on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoBase Succinylacetone Assay Solution Recalled by PerkinElmer Life and...
The Issue: There is a potential for leaking vials for certain lot numbers where, if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epi proColon Plasma Quick Kit Recalled by Epigenomics Ag Due to The...
The Issue: The diagnostic test kit may produce invalid test runs which may delay test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReNew Endocut Scissor Disposable Tip Recalled by Microline Surgical, Inc....
The Issue: Certain lots of disposable laparoscopic instrument tips may potentially have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE(TM) BRAND Recalled by 3M Company - Health Care Business Due to Mold was...
The Issue: Mold was found on the non-patient contact surfaces of the product and was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReNew Dolphin Nose Disposable Dissector Tip Recalled by Microline Surgical,...
The Issue: Certain lots of disposable laparoscopic instrument tips may potentially have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The internal...
The Issue: The internal configuration of the electrometers and the Real-Time control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to (1) Under...
The Issue: (1) Under certain conditions, if a malfunction alarm occurs while the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Mednet(TM) Medication Management Suite 6.1 and 6.21 Recalled by ICU...
The Issue: Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...
The Issue: Report was of an interrupted MR scan after patient complained about acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...
The Issue: L3 has determined in airport environments, there have been several cases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.