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. 1,029 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,029 in last 12 months

Showing 37241–37260 of 53,623 recalls

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· 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· 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· 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 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· 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
FoodMarch 8, 2016· Global Garlic, Inc.

Recalled Item: Ducal Apple Nectar Recalled by Global Garlic, Inc. Due to Florida Department...

The Issue: Florida Department of Agriculture and Consumer Services surveillance sample...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2016· Welle Pty Ltd

Recalled Item: The Super Elixir By WelleCo Australia Alkalising Greens 150g/5.3 oz net...

The Issue: Welle Pty Ltd is recalling Wellco Super Elixir pouches because of potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 7, 2016· Prayon Inc.

Recalled Item: Phosphoric Acid Recalled by Prayon Inc. Due to Potential contamination with...

The Issue: Potential contamination with trace levels of 1-methylethyl benze (more...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
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 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 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 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· 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· 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· 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· 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