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. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 29361–29380 of 52,000 recalls
Recalled Item: Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K Recalled by Beckman...
The Issue: Reagent carryover from Sekisui ACTH when utilized on the BEC AU 680 analyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Assay(R) Multi-Analyte Calibrator Recalled by Kamiya Biomedical Company,...
The Issue: The AlAT calibrator values in the package insert for the Multi-Analyte...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENICON EZEE Retrieval Recalled by Genicon, Inc. Due to Plastic handle is...
The Issue: Plastic handle is breaking off of shaft inhibiting proper removal per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pumpkin Seeds Recalled by TRULY GOOD FOODS Due to Undeclared Allergen
The Issue: Undeclared allergen Tree Nuts: Blackened Seasoned Pumpkin Seeds mixed up...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Voriconazole Tablets Recalled by AVKARE Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Out of specification for a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...
The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Elastic Esmark Bandage Recalled by Medline Industries Inc Due to...
The Issue: Product did not undergo correct sterilization procedures and may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...
The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...
The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 300 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...
The Issue: False blood back detection alarm and the ingress of fluids into the IABP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...
The Issue: False blood back detection alarm and the ingress of fluids into the IABP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100i Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...
The Issue: False blood back detection alarm and the ingress of fluids into the IABP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Product Usage: is a software system designed for treatment...
The Issue: For the proton QA preparation module in RayStation 6 (including SP1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: New Kopi Jantan Tradisional Natural Herbs Coffee Recalled by BESTHERBS...
The Issue: Marketed without an approved NDA/ANDA: presence of undeclared desmethyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.