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. 2,656 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,656 in last 12 months

Showing 2624126260 of 53,623 recalls

Medical DeviceAugust 12, 2018· The Binding Site Group, Ltd.

Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...

The Issue: A deterioration of performance was identified with influenza type B Enzyme...

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

Class II — Potential Health HazardOngoing
DrugAugust 10, 2018· Westlab Pharmacy, Inc. dba Westlab Pharmacy

Recalled Item: Cyclosporine 1% Human Eye Drops Recalled by Westlab Pharmacy, Inc. dba...

The Issue: Lack of Process Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2018· Westlab Pharmacy, Inc. dba Westlab Pharmacy

Recalled Item: ADAA Cataract Drops Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy...

The Issue: Lack of Process Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2018· Westlab Pharmacy, Inc. dba Westlab Pharmacy

Recalled Item: Alprostadil 500 mcg/mL Injectable Recalled by Westlab Pharmacy, Inc. dba...

The Issue: Incorrect Product Formulation

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2018· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...

The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.

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

Class III — Low RiskOngoing
Medical DeviceAugust 10, 2018· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: ev3 TurboHawk PERPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE Recalled by...

The Issue: The Distal Flush Tool (DFT) accessories that were packaged in this lot...

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

Class II — Potential Health HazardOngoing
DrugAugust 9, 2018· Orexigen Therapeutics, Inc.

Recalled Item: Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets...

The Issue: Defective Container: Customer complaints of punctures in the bottle.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 9, 2018· Besmed Health Business Corporation

Recalled Item: Ambu Aura40 Standard Recalled by Besmed Health Business Corporation Due to...

The Issue: Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Recalled...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 Recalled by...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2018· Akorn, Inc.

Recalled Item: Azelastine HCl Ophthalmic Solution 0.05% Recalled by Akorn, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications:out-of-specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy 3 Implant Recalled by Implant Direct Sybron...

The Issue: Two units in distribution were found to be mislabeled on the vial cap with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Philips North America LLC

Recalled Item: Philips HeartStart Infant/Child SMART Pads Cartridge Recalled by Philips...

The Issue: The recall is being initiated due to incorrect age range labeling (8+ yrs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Helena Laboratories, Corp.

Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...

The Issue: The positive control on some tests of the lots did not appropriately react...

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

Class II — Potential Health HazardOngoing