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 2112121140 of 29,505 recalls

Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Passer....

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Bit Recalled by...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. guide Recalled...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Applied Medical Resources Corp

Recalled Item: Direct Drive Clip Applier CA090 Recalled by Applied Medical Resources Corp...

The Issue: Increased customer complaints indicating inconsistent clip application; may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Recalled by B...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Smart CR Digital Computed Radiography System Recalled by Fujifilm Medical...

The Issue: Reports of failure of the device's power supply.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL-BIC Product...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item 3456103A The...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. cannula...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Orthopedic...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The Neonate Head protocol with the pediatric kernel Hp38 could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Arthroscope....

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Screw Recalled...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Spinal...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Rod Recalled by...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Uniqcot 1/2" x 2" : 67-29 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1.5" x 3" : 60-22 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing