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. 2,593 recalls have been distributed to Tennessee in the last 12 months.
Showing 18881–18900 of 29,188 recalls
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Recalled by Arrow...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "Pressure Injectable Jugular Axillo-Subclavian Central Catheter (JACC)...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath Recalled...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Catheterization Kit with Maximal Barrier Precautions The Arrow¿...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit The MAC(TM) Recalled...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology...
The Issue: When the Smart Check tool is used to perform a Smart Setup with one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation Recalled...
The Issue: Medtronic received reports that the DBS depth stop did not adequately secure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIZA Vertebral Body Replacement Recalled by Eden Spine Europe SA Due to...
The Issue: Complaints that implants have been disassembled by surgeons because of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ Administration Set Recalled by Smiths Medical ASD Inc. Due to Smiths...
The Issue: Smiths Medical has become aware that the drawing on the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Estradiol II Recalled by BioMerieux SA Due to Fulvestrant cross reacts...
The Issue: Fulvestrant cross reacts with the VIDAS Estradiol II immunoassay and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho Basic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altius M-INI OCT Posterior Spinal Fixation System Recalled by Zimmer Biomet...
The Issue: Zimmer Biomet is recalling the Altius M-INI OCT Posterior Spinal Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.