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. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 2736127380 of 29,505 recalls

Medical DeviceApril 17, 2013· DePuy Spine, Inc.

Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Recalled by DePuy Spine, Inc. Due to...

The Issue: During injection of cement, the water in the hydraulic pump leaks past the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· DePuy Spine, Inc.

Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM 11CC PLUS KIT Recalled by DePuy Spine, Inc....

The Issue: During injection of cement, the water in the hydraulic pump leaks past the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· Xlumena, Inc.

Recalled Item: Xlumena brand NAVIX Access Device Recalled by Xlumena, Inc. Due to A...

The Issue: A complaint investigation has found that product fractures can occur at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· DePuy Spine, Inc.

Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM KIT Recalled by DePuy Spine, Inc. Due to...

The Issue: During injection of cement, the water in the hydraulic pump leaks past the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· BioMerieux SA

Recalled Item: VIDAS D-Dimer Exclusion II Recalled by BioMerieux SA Due to Customer...

The Issue: Customer complaints about not repeatable results below the detection limit...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Ziemer Usa Inc

Recalled Item: 1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an Recalled by Ziemer Usa...

The Issue: A defect in the controller board can lead to the condenser to the video...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Alere San Diego, Inc.

Recalled Item: Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The Recalled by...

The Issue: The firm initiated recall of Alere" hCG Combo Cassette (20/10 mIU/mL) kit PN...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended...

The Issue: Bard Peripheral Vascular (BPV) has confirmed that some devices with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...

The Issue: Philips Healthcare received reports from the field that certain Brilliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic...

The Issue: AT rare, extremely high glucose levels (1024 mg/dL and above), the FreeStyle...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2013· Medrad Inc

Recalled Item: DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris Recalled by...

The Issue: The firm is recalling these power cables due to a latent design reliability...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Hill-Rom, Inc.

Recalled Item: Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been...

The Issue: Complaints have been reported for brakes disengaging when the bed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Hand Switch - Electric Pen Drive Recalled by Synthes USA HQ, Inc....

The Issue: Synthes received a complaint from a customer in which the Hand Switch for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Coloplast Manufacturing US, LLC

Recalled Item: Rostorelle L Recalled by Coloplast Manufacturing US, LLC Due to Mislabeling

The Issue: Coloplast is recalling one lot of Restorelle L prosthesis because it is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing