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. 2,666 recalls have been distributed to Tennessee in the last 12 months.
Showing 10261–10280 of 52,000 recalls
Recalled Item: allergy relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: allergyrelief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DeRoyal SafeLiner Suction Canister Recalled by DeRoyal Industries Inc Due to...
The Issue: The reason for the voluntary recall is due to shrinkage of the canister lid....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 App Recalled by Abbott Diabetes Care, Inc. Due to If using...
The Issue: If using affected glucose monitoring app on Android 13 Operating System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Flex: a) DBM S42090 GRAFTON 1.5CM X 1.5CM FLEX Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Accelerate Grafton DBF a) ACCELERATE BG SET T50203 GRAFTON DBF 3CC...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton DBF: a) PUTTY T50101 GRAFTON DBF 1CC Recalled by Medtronic...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Putty: a) DBM S43101 GRAFTON 0.5CC PUTTY Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Matrix Strips: a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Plus Paste a) DBM S45001 GRAFTON 1CC PASTE Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Orthoblend: a) DBM S44125 5CC ORTHOBLEND LARGE DEFECT...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Crunch a) DBM S44105 GRAFTON 5CC CRUNCH Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic XPANSE Bone Insert: a) DBM T600106 XPANSE SMALL-C 6 Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Gel: a) DBM S41120 GRAFTON GEL 1CC Recalled by Medtronic...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Matrix: a) DBM S42200 GRAFTON 2.5CMX10CM 2EA MATRIX...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton DBF Inject: a) GRAFTON T50303 DBF INJECT 3CC Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Presence of Foreign Tablets/Capsules: Presence of one Tacrolimus 1 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Hoffmann LRF Recalled by Stryker GmbH Due to Stryker has identified...
The Issue: Stryker has identified a nonconformance in specific lots of Hoffmann LRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.