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. 2,673 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,673 in last 12 months

Showing 2136121380 of 29,505 recalls

Medical DeviceMarch 9, 2016· Biomet, Inc.

Recalled Item: All instrumentation associated with the Prelude PF Resurfacing Knee System....

The Issue: Inadequate design control.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2016· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient...

The Issue: Panorama Central Station including the work station View Station, View...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva Emit Methotrexate Assay Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics confirmed that Syva Emit Methotrexate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· Pelton & Crane / Marus / DCI Equipment / KaVo

Recalled Item: Helios HL3T and HLT Track Mounted Dental Lights Product Usage: Recalled by...

The Issue: The firm received two customer complaints local Pelton & Crane distributors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· Hill-Rom, Inc.

Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....

The Issue: The center bolt of the sling bar, which connects the bar to the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Estradiol II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...

The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2016· MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK

Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...

The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...

The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2016· C.R. Bard, Inc.

Recalled Item: BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management...

The Issue: Complaints were received of restricted/inaccurate flow rate.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Extended Brilliance Workspace NM Special Nuclear medicine image display and...

The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Extended Brilliance Workspace NM Nuclear medicine image display and...

The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2016· Vascular Solutions, Inc.

Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...

The Issue: Vascular Solutions became aware of a potential problem with the click...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: The Spectra-System Dental Implant 2008 system is comprised of dental...

The Issue: Implant Direct Sybron Manufacturing, LLC is recalling GoDirect Implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IntelliSpace Portal DX/HX/EX AutoSPECT Pro Software Application Recalled by...

The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...

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

Class II — Potential Health HazardOngoing