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. 1,165 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,165 in last 12 months

Showing 2501–2520 of 29,505 recalls

Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE brand medical procedure kits labeled as: 1) ECONO Recalled by...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE CEMENT...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE SCHAMBERG...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE IUD Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE KOGAN...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Stryker Corporation

Recalled Item: 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000) 120V NEPTUNE S ROVER Recalled...

The Issue: Bolts on the vacuum pump filter housing and the flange plate were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE TROUSSEAU...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemo software Recalled by A L I Technologies...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: McKesson Cardiology Hemo software Recalled by A L I Technologies Ltd Due to...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Moximed, Inc.

Recalled Item: MISHA Knee System Implant Small Recalled by Moximed, Inc. Due to Knee...

The Issue: Knee implant may fracture due to a supplier-related issue with one component...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemodynamics software Recalled by A L I...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Accriva Diagnostics, Inc.

Recalled Item: VerifyNow P2Y12 Platelet Reactivity Test Recalled by Accriva Diagnostics,...

The Issue: Platelet Reactivity Test distributed without appropriate US-FDA market...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: X-Flow prostatectomy catheter Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: Folysil Silicone Foley Catheters Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoCove Putty Recalled by IsoTis OrthoBiologics, Inc. Due to Hydration...

The Issue: Hydration issue resulting in the product being less cohesive and moldable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix...

The Issue: Incorrect expiration date listed on the outer box, which does not align with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· 3M Unitek Corporation

Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...

The Issue: Due to an increase of complaints for bracket bond failures and skin...

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

Class II — Potential Health HazardOngoing