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. 2,831 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,831 in last 12 months

Showing 58415860 of 29,505 recalls

Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were identifying autofill failure conditions on the devices causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Wolf, Henke Sass, Gmbh

Recalled Item: Henke-Ject-2 part luer sterile single use syringes - used for intravenous...

The Issue: Sterile barrier might be damaged compromising the sterility of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Aomori Olympus Co., Ltd.

Recalled Item: Olympus Distal Attachment (in Olympus Disposable EMR Kit)- Designed to...

The Issue: The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which...

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

Class II — Potential Health HazardOngoing