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. 2,480 recalls have been distributed to Tennessee in the last 12 months.
Showing 32181–32200 of 52,000 recalls
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXAMETHASONE ELIXIR Recalled by Vintage Pharmaceuticals LLC dba Qualitest...
The Issue: Failed Impurities/ Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension...
The Issue: Labeling: Incorrect or missing package insert: the affected product was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5...
The Issue: A portion of this lot of blood collection tubes was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterFuse Tail Traction Tool Recalled by Vertebral Technologies, Inc. Due to...
The Issue: Fit issues have been identified with the Tail Traction Tool (PN 9116) when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway Recalled by...
The Issue: Labeling error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LIFEPAK 1000 defibrillator is intended for use by personnel Recalled by...
The Issue: The firm has received complaints that the LIFEPAK 1000 Defibrillator is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morning Life Recalled by Won Industry Co. Due to Distribution of unapproved...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compressible Limb Therapy System (Leg Cuffs Recalled by Won Industry Co. Due...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICTSWEET(R) FARMS Recalled by The Pictsweet Company Due to Product may...
The Issue: Product may contain glass fragments
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duopa (carbidopa and levodopa enteral suspension) Recalled by AbbVie Inc....
The Issue: Failed Stability Specifications: confirmed out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg Recalled by Sun...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Actavis Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product is out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System Recalled by Carestream Health...
The Issue: The firm received a complaint alleging that a DRX Revolution System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GrebSet Micro-Introducer Kit Recalled by Vascular Solutions, Inc. Due to...
The Issue: Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor Recalled by Physio-Control, Inc. Due to The firm has...
The Issue: The firm has become aware of a potential device issue where the LIFEPAK 15...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.