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. 2,638 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,638 in last 12 months

Showing 1438114400 of 29,188 recalls

Medical DeviceApril 12, 2019· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...

The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...

The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Tecan US, Inc.

Recalled Item: Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks...

The Issue: Gas springs not always replaced within the interval specified.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· OMNIlife science Inc.

Recalled Item: OMNIBotics iBlock Cutting Guide Recalled by OMNIlife science Inc. Due to The...

The Issue: The OMNIBotics iBlock Cutting Guide does not lock onto the iBlock Saw Guide...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2019· Intuitive Surgical Inc

Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical Inc Due to Failure...

The Issue: Failure of Universal Surgical Manipulators due to a high friction points,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2019· Intuitive Surgical Inc

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical Inc Due to...

The Issue: Failure of Universal Surgical Manipulators due to a high friction points,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2019· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling

The Issue: Certain lots were mislabeled with incorrect product number.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2019· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling

The Issue: Certain lots were mislabeled with incorrect product number.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing