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. 2,139 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,139 in last 12 months

Showing 56615680 of 29,505 recalls

Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2023· GE Healthcare

Recalled Item: Centricity Universal Viewer Workflow Manager Recalled by GE Healthcare Due...

The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2023· GE Medical Systems China Co., Ltd.

Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...

The Issue: There is a potential interruption of data communication between E-modules...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2023· GE Healthcare

Recalled Item: Universal Viewer Workflow Manager Recalled by GE Healthcare Due to When...

The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2023· Blue Belt Technologies, Inc

Recalled Item: Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software...

The Issue: CORI software was missing a planning stage that appears in cases of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number:...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing