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. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22681–22700 of 29,188 recalls
Recalled Item: VersaTREK Instrument Series 528 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Instrument Series 240 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Tni-Ultra Assay Recalled by Siemens Healthcare Diagnostics,...
The Issue: System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml Recalled by...
The Issue: A reduction in the reconstituted stability has been identified. Clinicians...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentraLink" Data Management System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has determined that the sample query function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/L Taper with Kinectiv¿ Technology. prosthesis Recalled by Zimmer, Inc. Due...
The Issue: Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearSight Recalled by Edwards Lifesciences, LLC Due to Edward Lifesciences...
The Issue: Edward Lifesciences is recalling the ClearSight System because the finger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 Recalled...
The Issue: Vial to vial variation in the fill volume that could affect control recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound, Inc. Due to Philips...
The Issue: Philips Healthcare has discovered a problem in the Philips Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROcise XP Wand with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure resulting in inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Search Circulating Tumor Kit. Intended for the enumeration of Recalled...
The Issue: Complaints of the presence of artifacts that appears as small bead like...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVAC 70 XTRA with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure causing device inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via and Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: measurements drawn on the 2nd and subsequent images of the series are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LapSac Surgical Tissue Pouch. The current intended use for the Recalled by...
The Issue: Includes Information not stated in the intended use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Optigun Ratchet is a hand-held cement gun for use Recalled by BIOMET...
The Issue: The pin which maintains the knob button, may disconnect and become lost....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson...
The Issue: The intake port may be blocked which can cause the bag to fail to fill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEDASYS Computer-Assisted Personalized Sedation System Recalled by Ethicon...
The Issue: Ethicon has found that disinfecting methods not specified in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws Recalled...
The Issue: Certain lots of the 3.7mm Cannulated Locking Screws and 3.7mm Cannulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Recalled by CareFusion 303, Inc. Due to An issue...
The Issue: An issue with the cancel functionality used during atypical infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm Cannulated Drill Bit/ QC 170 mm 2.7 Cannulated Recalled by Synthes,...
The Issue: affected parts and lots of the Cannulated Drill Bits have the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.