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. 2,593 recalls have been distributed to Tennessee in the last 12 months.
Showing 18741–18760 of 29,188 recalls
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N235) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N276) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Frequency Resection Electrodes Recalled by Olympus Corporation of the...
The Issue: Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent...
The Issue: Firm has identified that ARCHITECT SHBG results generated with the Potassium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...
The Issue: nail not properly engaging with the targeting jig due to certain undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonabsorbable suture anchor system intended to reattach soft tissue to...
The Issue: Manufactured with the incorrect anchor outer body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...
The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Aquasonic 100 Ultrasound Transmission Gel Recalled by Parker...
The Issue: There is a potential for the gel packets to have leaks in the packet seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...
The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...
The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI . The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dolphin Inflation Device Recalled by Vascular Solutions, Inc. Due to The...
The Issue: The manufacturer of the DOLPHIN inflation device, Perouse Medical, has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...
The Issue: An unexpected transient mode switch behavior was detected by Medtronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...
The Issue: An extremely dusty computer can cause problems at system start, or rarely,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.