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. 2,686 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,686 in last 12 months

Showing 2042120440 of 29,505 recalls

Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: 5 Port OFF Manifold with Transpac IV Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir and 2 Recalled...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Triple Line SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Bifurcated SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with 84" SafeSet Reservoir Recalled...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with SafeSet 84" Arterial Pressure Tubing...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Monitoring Kit with TP4 Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 03 ml Squeeze Flush Recalled by ICU Medical,...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Bifurcated Kit with SafeSet Reservoir Recalled by ICU Medical,...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet 84" Arterial Pressure Tubing...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 Recalled by Mentor...

The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...

The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 Recalled by Mentor...

The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders...

The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...

The Issue: Communication provided to emphasize that the PSA values should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Zimmer Biomet, Inc.

Recalled Item: Phoenix Recon Soft Tissue Sleeve Guide Recalled by Zimmer Biomet, Inc. Due...

The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Zimmer Biomet, Inc.

Recalled Item: Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Recalled by...

The Issue: Contents of the package do not match the product labeling. Product is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Zimmer Biomet, Inc.

Recalled Item: Phoenix Recon Targeting Arm Guide Recalled by Zimmer Biomet, Inc. Due to Old...

The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Swissray Medical

Recalled Item: ddR Formula B X-ray System Recalled by Swissray Medical Due to Possible...

The Issue: Possible injury due to movement of the arm, calibration loss and...

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

Class II — Potential Health HazardOngoing