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. 2,743 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,743 in last 12 months

Showing 1752117540 of 53,623 recalls

Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
FoodFebruary 3, 2021· Ocean Beauty Seafoods LLC

Recalled Item: The RETAIL package is black cardboard box and product is Recalled by Ocean...

The Issue: Undeclared Soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 3, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable cardioverter defibrillators (ICD) with cardiac resynchronization...

The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2021· LumiraDx

Recalled Item: Coronavirus antigen detection test system - Product Usage: intended for...

The Issue: Two lots of test strips failed QC testing using blank buffer due to false...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR...

The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista HDLC - colorimetric method Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for...

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Apotex Corp.

Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...

The Issue: Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 2, 2021· Apotex Corp.

Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...

The Issue: Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2021· Philips North America Llc

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America Llc Due to...

The Issue: Manufacturing failed to follow process steps resulting in the distribution...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2021· Alcon Research, LLC

Recalled Item: Alcon Custom Ophthalmic Surgical Procedure Packs Recalled by Alcon Research,...

The Issue: Reports have been received concerning mold found on gowns included in custom...

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

Class II — Potential Health HazardOngoing
DrugFebruary 1, 2021· Kimberly-Clark Corporation

Recalled Item: Scott¿ Moisturizing Foam Hand Sanitizer Recalled by Kimberly-Clark...

The Issue: Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 1, 2021· Epimed International, Inc.

Recalled Item: Feth-R-Kath Catheter Recalled by Epimed International, Inc. Due to Outer...

The Issue: Outer coating of the catheter may deteriorate and result in the coating to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2021· Bovie Medical Corporation

Recalled Item: Velocity Disposable Bipolar Ablators - Product Usage: intended to be...

The Issue: There can be a potential breach of the sterile packaging barrier due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2021· Bovie Medical Corporation

Recalled Item: ConMed Disposable Bipolar Ablators - Product Usage: intended to be Recalled...

The Issue: There can be a potential breach of the sterile packaging barrier due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2021· Bovie Medical Corporation

Recalled Item: HNM Disposable Bipolar Ablators - Product Usage: intended to be used for...

The Issue: There can be a potential breach of the sterile packaging barrier due to the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2021· Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
FoodJanuary 29, 2021· Renaissance Food Group, LLC

Recalled Item: BUFFALO STYLE CHICKEN Sliders NET WT. 5OZ (141g) Ingredients: Tuna Recalled...

The Issue: The firm was notified by a customer that the Buffalo Style Chicken Sliders...

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

Class II — Potential Health HazardOngoing
Refund