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. 2,837 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,837 in last 12 months

Showing 47814800 of 53,623 recalls

Medical DeviceAugust 30, 2024· Blue Ortho

Recalled Item: Predict+ is a data-driven Recalled by Blue Ortho Due to Predict+ is being...

The Issue: Predict+ is being recalled for lack of pre-market clearance/approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Melrose Wakefield Hospital Injector And Syringe Recalled by Merit Medical...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar Injector And Syringe Recalled by Merit...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP403 MBA Hemostasis Valve Metal...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP302 Honor Hemostasis Valve Metal...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Automatic Digital Blood Pressure Monitor Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device MAP 112 Access-9 Large Bore Hemostasis Value...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Stryker Neurovascular

Recalled Item: The Trevo Trak 21 Microcatheter is a single-lumen Recalled by Stryker...

The Issue: Stryker Neurovascular has observed that devices with Out of United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to The...

The Issue: The software has anomalies that have the potential to cause alarms,...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 30, 2024· Philips North America

Recalled Item: IntelliVue Patient Monitor MX400 (Model Number 866060) Recalled by Philips...

The Issue: During a production process, Philips became aware of one IntelliVue power...

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

Class II — Potential Health HazardOngoing
FoodAugust 29, 2024· Niitakaya USA Inc

Recalled Item: Miso Katsuo Ninniku (Pickled Garlic) Recalled by Niitakaya USA Inc Due to...

The Issue: Undeclared allergen (Fish) Ingredient

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 29, 2024· Niitakaya USA Inc

Recalled Item: Shiso Katsuo Ninniku (Pink Pickled Garlic) Recalled by Niitakaya USA Inc Due...

The Issue: Undeclared allergen (Fish) Ingredient

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2024· Wilson-Cook Medical Inc.

Recalled Item: Cook Medical Hemo-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook...

The Issue: Specific lots of product have been manufactured with nonconforming raw...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· CooperVision, Inc.

Recalled Item: Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for...

The Issue: Manufactured with a misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· CooperVision, Inc.

Recalled Item: BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for Recalled by...

The Issue: Manufactured with a misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· Tornier, Inc

Recalled Item: Stryker Tornier Perform Humeral System Recalled by Tornier, Inc Due to...

The Issue: Devices from one lot of Perform" Reversed Inserts may contain a locking ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· Microcare Medical

Recalled Item: Good Vibrations Ultrasonic Cleaner Solution Recalled by Microcare Medical...

The Issue: Contaminated equipment and packaging caused Klebsiella oxytoca, Enterobacter...

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

Class II — Potential Health HazardOngoing