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. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 2946129480 of 53,623 recalls

Medical DeviceNovember 8, 2017· Bard Medical Division

Recalled Item: Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description Recalled by Bard...

The Issue: Specific lots of ArcticGel Pads have potential issues which may result in...

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

Class II — Potential Health HazardOngoing
DrugNovember 6, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...

The Issue: Superpotent

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

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

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

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

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

Class III — Low RiskOngoing
Refund
FoodNovember 6, 2017· Pacific Rim Distribution Inc.

Recalled Item: Bean Boy Coffee Dark Chocolate Covered Espresso Beans Recalled by Pacific...

The Issue: Pacific Rim Distribution Inc., dba Bean Boy Coffee is voluntarily recalling...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 6, 2017· Boston Scientific Corporation

Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...

The Issue: Stent possibly unable to be fully released from the delivery system.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· Boston Scientific Corporation

Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...

The Issue: Stent possibly unable to be fully released from the delivery system.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...

The Issue: Device may potentially be compromised by water in end user packaging....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...

The Issue: Device may potentially be compromised by water in end user packaging....

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

Class II — Potential Health HazardOngoing
DrugNovember 3, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: bupPROPion HCL Extended-Release Tablets Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Mylan Pharmaceuticals Inc. is...

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

Class III — Low RiskOngoing
Refund
FoodNovember 3, 2017· Gourmet Nut, Inc.

Recalled Item: GourmetNut DARK CHOCOLATE COVERED ALMONDS NET WT 7oz (198g) Recalled by...

The Issue: Product contains undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: NovaKone Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden Classic 38 Sphere Daily Wear Soft contact Recalled by Alden Optical...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP59 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing