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. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1272112740 of 29,188 recalls

Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 27G Blunt Needles with luer-lock connector-.D05 GTIN:8719214221669...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...

The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Smith & Nephew, Inc.

Recalled Item: LEGION AP Cutting Block Size 4 Recalled by Smith & Nephew, Inc. Due to...

The Issue: Multiple lots of LEGION AP Femoral Cutting Blocks were manufactured with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...

The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· Beckman Coulter Inc.

Recalled Item: Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled by Beckman...

The Issue: Due to customer reports it has been determined that the inoculation system...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System Recalled by TELEFLEX...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· CooperSurgical, Inc.

Recalled Item: ADVANCED ENDOSEE System CANNULA Recalled by CooperSurgical, Inc. Due to...

The Issue: Potential for unsealed pouches in two (2) lots of the Endosee Advance...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2019· ResMed Ltd.

Recalled Item: ResMed Stellar Recalled by ResMed Ltd. Due to Combination of software and a...

The Issue: Combination of software and a component failure may cause audible alarms not...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: Clearlink System Continu-Flo Administration Sets Recalled by Baxter...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: ONE-LINK Needle-free IV Connector Recalled by Baxter Healthcare Corporation...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Health Network Strips- intended for Blood Glucose...

The Issue: Inability to dose the test strips, may result in a temporary inability to...

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

Class II — Potential Health HazardOngoing