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. 2,563 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,563 in last 12 months

Showing 4324143260 of 53,623 recalls

Medical DeviceDecember 4, 2014· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...

The Issue: There is the potential for a breach in the inner or outer packaging pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Zimmer Manufacturing B.V.

Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...

The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...

The Issue: There is the potential for a breach in the inner or outer packaging pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...

The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...

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

Class II — Potential Health HazardOngoing
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops Advanced Relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops A.C. (Tetrahydrozoline HCl 0.05% Recalled by K C Pharmaceuticals...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Micro Labs Usa, Inc S

Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product failed a known...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Baxter Healthcare Corp

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaints received for...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops Industrial Strength (Polyethylene glycol 400 1% Recalled by K C...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Micro Labs Usa, Inc S

Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product failed a known...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops (Tetrahydrozoline HCl 0.05%) Recalled by K C Pharmaceuticals Inc...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Micro Labs Usa, Inc S

Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product failed a known...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2014· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2014· Hospira Inc.

Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...

The Issue: Failed Stability Specifications: Product is subpotent and has out of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 3, 2014· Iris Diagnostics

Recalled Item: RTH8 Rotor Recalled by Iris Diagnostics Due to Iris International is...

The Issue: Iris International is recalling the RTH8 Rotor used in the StatSpin Express...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Ferno-Washington Inc

Recalled Item: Ferno Model 35X PROFlexx Stretchers Recalled by Ferno-Washington Inc Due to...

The Issue: The wheel castor assemblies may be loosening on the stretchers.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Medtronic Sofamor Danek USA Inc

Recalled Item: POWEREASE Instruments Set Screw Breakoff Instrument Recalled by Medtronic...

The Issue: The retaining tabs component of the Set Screw Retaining Drive may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Teleflex Medical

Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...

The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...

The Issue: Suboptimal routing of the cable may result in increased wear over time....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing