Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,768 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,768 in last 12 months

Showing 1452114540 of 29,505 recalls

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
Medical DeviceApril 10, 2019· Uromedica Inc.

Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...

The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...

The Issue: The firm has become aware of a potential problem that their Catheters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...

The Issue: The firm has become aware of a potential problem that their Catheters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Becton Dickinson & Company

Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...

The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· QUIDEL CARDIOVASCULAR INC

Recalled Item: Quidel Triage TOX Drug Screen Control 1 Kit Box containing Recalled by...

The Issue: Due to an error in the programming of the Control CODE CHIP module for this...

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

Class II — Potential Health HazardOngoing