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 1510115120 of 29,188 recalls

Medical DeviceOctober 31, 2018· Foundation Medicine, Inc.

Recalled Item: FoundationOne CDx Test Results Recalled by Foundation Medicine, Inc. Due to...

The Issue: An incorrect test result for a single analyte may have been reported for up...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Zimmer Biomet, Inc.

Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...

The Issue: Screw is missing from the package

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· COVIDIEN LLC

Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...

The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2018· Horiba Instruments Incorporated

Recalled Item: Clinical Chemistry Recalled by Horiba Instruments Incorporated Due to...

The Issue: Potential for chemical analyzer to report abnormal results due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2018· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...

The Issue: There is a potential for blood leakage at the blood inlet connector when...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2018· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...

The Issue: There is a potential for blood leakage at the blood inlet connector when...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Instrument Arm Drape. QTY 1 Pouch Recalled by Intuitive...

The Issue: The instrument drape may tear while draping the Patient Side Cart presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...

The Issue: Potential metal burrs in the holes of the device preventing the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire - Bullet Tip Recalled...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage:...

The Issue: Inspection process at the manufacturer found nonwoven material was used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Humeral Guide Wire - Ball Tip Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 128 Multi-slice CT Scanner System Product Usage: The Multi-Slice...

The Issue: Software defect: For Helical scan with ClearView function, when small arc...

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

Class II — Potential Health HazardOngoing