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. 2,401 recalls have been distributed to Tennessee in the last 12 months.
Showing 44301–44320 of 52,000 recalls
Recalled Item: Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco Pharmaceutical...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bissinger's Dark Chocolate Bunny Ears Recalled by Karl Bissinger LLC Due to...
The Issue: Milk chocolate bunny ears are packaged in dark chocolate packaging. The...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...
The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...
The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae Recalled by...
The Issue: Potential for separation of dilator tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...
The Issue: Potential for separation of dilator tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules Recalled by Pfizer Inc. Due...
The Issue: Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...
The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...
The Issue: There is a potential for patient finger injury on the e.cam systems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...
The Issue: In special cases, during the start-up of the current model of MobileDiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sevoflurane Recalled by Piramal Critical Care, Inc. Due to Failed pH...
The Issue: Failed pH Specifications: product was too acidic.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natural Grocers by Vitamin Cottage Recalled by Natural Grocers by Vitamin...
The Issue: Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado based...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...
The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...
The Issue: Separation events have occurred, including the VIPR separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glucose Hexokinase Liquid Reagent For the in vitro quantitative...
The Issue: JAS Diagnostics, Inc. of Miami Lakes, FL is recalling their Glucose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...
The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azathioprine Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.