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.
Showing 17941–17960 of 53,623 recalls
Recalled Item: Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use...
The Issue: Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FUJIFILM Synapse PACS Software: versions 7.0.0 and 7.0.1 - Product Recalled...
The Issue: The software does not update measurements and calculations in the Clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended...
The Issue: The electrical contactor component present in the drying chamber of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERITAS Collagen Matrix - Product Usage: intended for use in Recalled by...
The Issue: VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CKMB Slides: (1)VITROS CKMB Slides (60 Slide...
The Issue: VITROS Chemistry Products CKMB Slides Potential for Falsely Elevated Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...
The Issue: Subpotent Drug: Low out-of-specification assay results for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SenTec Digital Monitor Recalled by SenTec AG Due to Device requires the use...
The Issue: Device requires the use of an Isolation Transformer in combination with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 600FP Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has become aware of a potential safety issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Blood Agar/MacConkey Agar Bi-Plate Recalled by Remel Inc Due to The...
The Issue: The blood agar side of the bi-plate may not grow some patient isolates or QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clerio Vision Recalled by Clerio Vision Due to One lot of contact lenses...
The Issue: One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment Delivery System with iDMS - Product Usage: used...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System - Product Usage: used as an integrated Recalled...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxyzine Hydrochloride Oral Solution Recalled by Morton Grove...
The Issue: Failed Impurities/Degradation Specification: OOS for the following - unknown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.