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. 2,637 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,637 in last 12 months

Showing 1518115200 of 29,188 recalls

Medical DeviceOctober 11, 2018· St. Jude Medical, Inc.

Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....

The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...

The Issue: It was identified that the volume of air inside the mattress may expand in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...

The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2018· Theragenics Corporation

Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...

The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Synaptive Medical Inc

Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...

The Issue: This recall has been initiated due to a software defect found in the Guide...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 8, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Recalled by...

The Issue: VITROS Chemistry Products dLDL Reagent GENs 26 and 27, negatively biased results

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: The Spirit Plus Bed Recalled by Stryker Medical Division of Stryker...

The Issue: The beds with the high rail side rail option may not be complaint with IEC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· bioMerieux, Inc.

Recalled Item: bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134 Recalled by...

The Issue: Some eluates become colored because of remaining hemoglobin in the eluate.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: The Spirit Select Bed Recalled by Stryker Medical Division of Stryker...

The Issue: The beds with the high rail side rail option may not be complaint with IEC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Ohmeda Medical

Recalled Item: Giraffe Omnibed - Product Usage: The OmniBed is a combination Recalled by...

The Issue: GE Healthcare has become aware of a potential safety issue that can occur if...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· ICU Medical, Inc.

Recalled Item: Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1...

The Issue: Potential for leakage due to defect in the thermoset check valve component.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· ICU Medical, Inc.

Recalled Item: Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit...

The Issue: Potential for leakage due to defect in the thermoset check valve component.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· ICU Medical, Inc.

Recalled Item: Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1...

The Issue: Potential for leakage due to defect in the thermoset check valve component.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Tosoh Bioscience Inc

Recalled Item: Hemoglobin A1c Control Recalled by Tosoh Bioscience Inc Due to Tosoh...

The Issue: Tosoh Bioscience has become aware of potential degradation of HbA1c control...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 5, 2018· GE Healthcare, LLC

Recalled Item: GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard Recalled by GE...

The Issue: The ventilator Inspiratory Safety Guard (ISG) may disconnect from the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing