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. 2,520 recalls have been distributed to Tennessee in the last 12 months.
Showing 23961–23980 of 29,188 recalls
Recalled Item: Remel TB Potassium Permanganate (.5% Aqueous) 40192 Recalled by Remel Inc...
The Issue: The product may appear cloudy or discolored and may not perform correctly in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...
The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...
The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...
The Issue: It was determined that if the Mammomat Inspiration system is not secured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The J700 Floor Mounted Tube Stand (FMTS) is intended to Recalled by Summit...
The Issue: The welds on J700 tube stands may be insufficient resulting in tube stand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...
The Issue: Portions of the lots may contain units with an incorrect lens axis condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...
The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...
The Issue: Drill set may contain incorrect drill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...
The Issue: Potential breach of sterile barrier due to defective product tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some...
The Issue: Some material of the coating Type CXCPMV3 has potential artifacts showing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Titan Reverse Shoulder System right and left head cutting templates...
The Issue: A single lot of left and a single lot of right Reverse Shoulder System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Relief ACP Oral Care Gel intended to relieve discomfort from Recalled by...
The Issue: Product sold after April 1, 2014 were inadvertently filled with hydrogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nerve Block Tray (Nerve Block convenience kit) Recalled by Centurion Medical...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Imaging Tray (General Surgery convenience kit) Recalled by...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTROL P Control for ROTEM delta Thromboelastometry System Recalled by TEM...
The Issue: Some of vials were found to be partially filled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott m2000sp Recalled by Abbott Molecular Due to Some versions of...
The Issue: Some versions of Application Specifications (App Spec) are incompatible with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Pneumo Groups 2-14 Latex Test Recalled by Remel Inc Due to...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.