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. 2,730 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,730 in last 12 months

Showing 1848118500 of 53,623 recalls

FoodOctober 1, 2020· Desert Premium Group, LLC

Recalled Item: Trader Joe's Hatch Valley Salsa Recalled by Desert Premium Group, LLC Due to...

The Issue: One batch of salsa had a recorded equilibrium pH of 6.65.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...

The Issue: Potential contamination with S. epidermidis E. coli and S. warneri.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Recalled by...

The Issue: Potential contamination with Escherichia coli Staphylococcus epidermidis and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: LYFO DISK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...

The Issue: Potential contamination with Escherichia coli, Staphylococcus epidermidis...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...

The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...

The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...

The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Merz North America, Inc.

Recalled Item: COAPTITE Injectable Implant Recalled by Merz North America, Inc. Due to The...

The Issue: The Instructions for Use (IFU) updated 03/02/2020 does not match data listed...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Blood Monitoring Unit (BMU 40) Recalled by Maquet Cardiovascular Us Sales,...

The Issue: The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2020· Verathon, Inc.

Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...

The Issue: Due to a change in handle material and process, probe handle may crack.

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2020· Teligent Pharma, Inc.

Recalled Item: Fluocinonide Ointment USP 0.05% Recalled by Teligent Pharma, Inc. Due to...

The Issue: Failed Impurities/Degradation - Out-of-specification results for...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 28, 2020· Hormel Foods Corporation

Recalled Item: SKIPPY Super Chunk Peanut Butter 16.3oz packaged in Recalled by Hormel Foods...

The Issue: Aflatoxin level slightly above actionable limit

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2020· Advanced Bionics, LLC

Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...

The Issue: Mislabeling; It has been determined that some batteries were improperly...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2020· Advanced Bionics, LLC

Recalled Item: AB PowerCel 230 (velvet black) Recalled by Advanced Bionics, LLC Due to...

The Issue: Mislabeling; It has been determined that some batteries were improperly...

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

Class III — Low RiskOngoing
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Happy Ducts Compress Recalled by Wishgarden Herbs, Incorporated Due to...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Goldenseal POWDER Recalled by Wishgarden Herbs, Incorporated Due to...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Cord Care POWDER Recalled by Wishgarden Herbs, Incorporated Due to Microbial...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· VistaPharm, Inc.

Recalled Item: NYSTATIN ORAL SUSPENSION Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurties/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 25, 2020· Stryker GmbH

Recalled Item: Osteosynthesis Compression Staple EasyClip Recalled by Stryker GmbH Due to...

The Issue: The device has the potential to release nickel above the acceptable margin...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2020· Quidel Corporation

Recalled Item: QUIDEL Sofia SARS Antigen FIA IVD Recalled by Quidel Corporation Due to Due...

The Issue: Due to false positive results.

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

Class II — Potential Health HazardOngoing