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. 2,710 recalls have been distributed to Tennessee in the last 12 months.
Showing 961–980 of 52,000 recalls
Recalled Item: Lanthanum Carbonate chewable tablets Recalled by Cipla USA, Inc. Due to...
The Issue: Failed stability specifications: Out of specification for hardness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAMMOMAT Inspiration Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There were instances where the operator table was sold together with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMMOMAT Fusion Recalled by Siemens Medical Solutions USA, Inc Due to There...
The Issue: There were instances where the operator table was sold together with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There were instances where the operator table was sold together with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bakery Graham Pieces Recalled by Ice Cream Factory, LLC Due to Foreign...
The Issue: Foreign material fragments consisting of aluminum foil and packaging...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Strawberry Cheesecake Ice Cream with graham crackers swirl Recalled by Ice...
The Issue: Foreign material fragments consisting of aluminum foil and packaging...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bromocriptine Mesylate Capsules Recalled by Zydus Pharmaceuticals (USA) Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiosave Rescue Recalled by Datascope Corp. Due to The IFU addendum...
The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Recalled by Datascope Corp. Due to The IFU addendum...
The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Kiestra" Isolate Suspension Cuvette Array Recalled by Becton Dickinson &...
The Issue: The 2D barcodes on these cuvettes contain formatting errors that prevent the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.