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. 1,147 recalls have been distributed to Tennessee in the last 12 months.
Showing 2101–2120 of 52,000 recalls
Recalled Item: Ingenia Ambition S Model Numbers (REF): (1) 781359 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700 Model Number (REF): 782130 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR Recalled by Philips North America Due to The potential for...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 5300 Model Numbers (REF): (1) 782110 Recalled by Philips North America...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118 Recalled by...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 3.0T Quasar Dual Model Number (REF): 781150 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Model Numbers (REF): (1) 782120 Recalled by Philips North America...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Model Numbers (REF): (1) 781315 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED Recalled by...
The Issue: Cannulated fenestrated polyaxial screws may be incorrectly labeled
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Model Numbers (REF): (1) 781271 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buffered Penicillin G Potassium for Injection Recalled by Sandoz Inc Due to...
The Issue: Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin for Injection Recalled by Sandoz Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: clomiPRAMINE Hydrochloride Capsules USP 25 mg Recalled by Lupin...
The Issue: Failed Impurities/Degradation Specifications: an out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fudge Frenzy Bar (86210) Recalled by Rich Ice Cream Co Due to Potential...
The Issue: Potential Listeria Monocytogenes Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.