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. 2,819 recalls have been distributed to Georgia in the last 12 months.
Showing 9141–9160 of 29,505 recalls
Recalled Item: ARCH Leg Positioning System Recalled by Innovative Orthopedic Technologies,...
The Issue: Due to the holes not being bored to the specific diameter, the locking pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIVE S 3.5x65 Recalled by Karl Storz Endoscopy Due to During a regular...
The Issue: During a regular requalification review, affected flexible intubation video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foundation Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare Due...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Pack Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Easi-Care Gait Belt Metal Buckle (54" Recalled by Kinsman Enterprises Inc...
The Issue: The belt may fail at lower loads than the labeled 600lbs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenaculum Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endometrial Biopsy Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
The Issue: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) Recalled by Inpeco S.A. Due to The Firmware (FW) of the...
The Issue: The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoHelical and TomoDirect plans in RayStation 6 Recalled by RAYSEARCH...
The Issue: If the dynamic jaw mode is used and an optimization is continued after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee Recalled by...
The Issue: Packaging may include screws that are not intended to be used with the 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nexiva Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to...
The Issue: There is a breach in the product packaging that renders the product non-sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.