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. 2,637 recalls have been distributed to Tennessee in the last 12 months.
Showing 14401–14420 of 29,188 recalls
Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...
The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...
The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: Recalled...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.