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. 2,842 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,842 in last 12 months

Showing 42014220 of 29,505 recalls

Medical DeviceApril 15, 2024· Maquet Medical Systems USA

Recalled Item: CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system....

The Issue: The firm identified that the measured patient leakage current in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Philips North America Llc

Recalled Item: Incisive CT - Computed Tomography X-Ray System intended to produce Recalled...

The Issue: Metal mounting box on the rotating scanner on rotor (heat change box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Philips North America Llc

Recalled Item: Incisive CT - Computed Tomography X-Ray System intended to produce Recalled...

The Issue: Metal mounting box on the rotating scanner on rotor (heat change box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2024· Medartis Inc.

Recalled Item: APTUS 2.8 TriLock Screw 22mm Recalled by Medartis Inc. Due to Screw is 16mm...

The Issue: Screw is 16mm long instead of 22mm long.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2024· Securitas Healthcare LLC

Recalled Item: Arial mobile application Recalled by Securitas Healthcare LLC Due to The...

The Issue: The Arial Mobile Application utilizing Apple iOS 17.4 and iOS 17.5 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: FDR Visionary Suite - Intended to generate digital or conventional Recalled...

The Issue: Bolts on the CH-200 tube may rupture due to fatigue failure, causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Noblus AC Adapter used with the Noblus Ultrasound Imaging System Recalled by...

The Issue: AC adapters of Noblus can heat up, and cause smoke in the worst case, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS Tissue Processor Recalled by LEICA BIOSYSTEMS...

The Issue: Poorly processed and/or damaged biopsy tissue specimens on the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· GE Medical Systems Information Technologies Inc

Recalled Item: GE HealthCare CRITIKON ONE-CUF blood pressure cuffs Recalled by GE Medical...

The Issue: Use of the blood pressure cuffs could result in inaccurate non-invasive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Calibrators-IVD are for use with...

The Issue: Free T3 Calibrators used with T3 Reagent Packs may produce positively biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum IQ Infusion pump Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential for cracks on the mount of the front panel of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the...

The Issue: T3 Reagent Packs used with Free T3 Calibrators may produce positively biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) NEPHROLOGY PACK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) CONTINUOUS BLOCK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Novalung sensor box is a component of the Novalung Console Recalled by...

The Issue: Issue related to Novalung sensor box, which is a component of the Novalung...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2024· HeartSine Technologies Ltd

Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator) Recalled by HeartSine...

The Issue: Automated external defibrillators have a manufacturing issue that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2024· Vyaire Medical, Inc.

Recalled Item: Vyaire Medical GmbH Recalled by Vyaire Medical, Inc. Due to Potential of the...

The Issue: Potential of the nozzle separating during patient use.

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

Class I — Serious Health HazardOngoing