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. 2,549 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,549 in last 12 months

Showing 5320153220 of 53,623 recalls

DrugFebruary 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...

The Issue: Presence of Foreign Substance(s): There is a potential for foreign...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...

The Issue: Presence of Foreign Substance(s): There is a potential for foreign...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2012· Maquet Cardiovascular Us Sales, Llc

Recalled Item: FLOW-I Anesthesia System The system is intended for use in Recalled by...

The Issue: A technical alarm may be generated on the FLOW-i system when using the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 20, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: enFlow IV Fluid Warmer (510k name: EFLOW IV FLUID WARMER Recalled by Vital...

The Issue: The EnFlow Warmer Strap does not meet the requirements of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module with v2.0 software used Recalled...

The Issue: GE Healthcare became aware of two issues with the Patient Data Module using...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2012· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle Recalled by...

The Issue: A Discrepancy was found on Hitachi AST (HA7 61) package insert. Limitations...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 12, 2012· Ossur Americas, Inc.

Recalled Item: The Symbionic Leg is an integrated prosthetic leg for transfemoral Recalled...

The Issue: OSSUR initiated this recall of the Symbionic Leg because it may have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Integra LifeSciences Corp.

Recalled Item: Integra¿ Advansys Medial Lisfranc Plate (MLP) Recalled by Integra...

The Issue: Incorrect technique applied may cause potential rupture of the tibialis...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2012· Physicians Total Care, Inc.

Recalled Item: Lipitor (Atorvastatin calcium) Recalled by Physicians Total Care, Inc. Due...

The Issue: Chemical Contamination: Complaints of an uncharacteristic odor identified as...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2012· Afassco Inc

Recalled Item: The finger cots are made out of natural rubber. They Recalled by Afassco Inc...

The Issue: The firm is initiating a field correction because the product(s) were...

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

Class II — Potential Health HazardOngoing
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2012· Metrex Research, LLC.

Recalled Item: CaviCide Recalled by Metrex Research, LLC. Due to Metrex Research is...

The Issue: Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2012· Accumetrics Inc

Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...

The Issue: The recall was initiated by Accumetrics because of a field correction to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2012· Accumetrics Inc

Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...

The Issue: The recall was initiated by Accumetrics because of a field correction to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing