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. 1,036 recalls have been distributed to Tennessee in the last 12 months.
Showing 21641–21660 of 52,000 recalls
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Camera Recalled by Intuitive Surgical, Inc. Due to Some cameras...
The Issue: Some cameras were found to have residual soil adhered to the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...
The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by...
The Issue: It has been determined that some units of catheters were not tightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...
The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for Recalled by SCA...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 83 mm Item # 195253 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 63mm Item # 195269 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 69 mm Item # 195248 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 91mm Item # 195761 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...
The Issue: A patch was released for a critical remote code execution vulnerability in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 73mm Item # 195274 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 75 mm Item # 195757 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.