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. 2,656 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,656 in last 12 months

Showing 2478124800 of 29,505 recalls

Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw 32 mm Thread Length Sterile zimmer Recalled by...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Abbott Laboratories

Recalled Item: ICT Serum Calibrator . For use in the calibration Recalled by Abbott...

The Issue: ICT Serum Calibrator may generate lower than expected Potassium Quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· GF Health Products, Inc./d.b.a.Basic American Metal Products

Recalled Item: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...

The Issue: The bed head deck may fail to elevate as expected during normal operation....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...

The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Diagnostica Stago, Inc.

Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....

The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· BD Biosciences, Systems & Reagents

Recalled Item: BD Multi Check CD4 Low Control Catalog No. 340916 is Recalled by BD...

The Issue: The outer box label contains the incorrect distribution date: Box states...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Vital Sync RMS 1.0 when loaded with v2.4 software Recalled by Nellcor...

The Issue: Covidien is conducting a field correction of the Vital Sync Virtual Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Zimmer, Inc.

Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Cook Inc.

Recalled Item: CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a...

The Issue: This remedial action is the result of six product complaints associated with...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Vital Sync" VPMP & IM Recalled by Nellcor Puritan Bennett Inc. (dba Covidien...

The Issue: Covidien is conducting a field correction of the Vital Sync Virtual Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs...

The Issue: Customers may receive positively biased results when using VITROS¿...

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

Class II — Potential Health HazardOngoing