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. 2,643 recalls have been distributed to Georgia in the last 12 months.
Showing 26781–26800 of 29,505 recalls
Recalled Item: Pipeline Embolization Device (PED) The Pipeline Embolization Device is...
The Issue: Covidien Neurovascular has initiated the recall of several lots of Pipeline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR TacShield Mesh (All sizes and shapes). Intended for use Recalled by...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue...
The Issue: Blue Belt Technologies is recalling sterile Monitor Drapes used with their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR V-Patch Mesh (All sizes and shapes). Intended for use Recalled by...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distributed in USA: Product Number: 40-2894: Reinforced Wound Closure...
The Issue: Aspen Surgical is recalling Wound Closures because firm could not confirm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...
The Issue: Siemens has become aware of a customer complaint concerning the rail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Temperature Probes Recalled by Vital Signs Devices, a 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: Medtronic Custom Perfusion System. Model Numbers: 1D80R8 Recalled by...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Leyla Ball Joint Clamp Recalled by Integra Limited Due to As a...
The Issue: As a result of complaint investigations it was identified that there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion System with Trillium BioSurface (a polymer...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter...
The Issue: Arrow is recalling the Arrowgard Blue Plus Antimicrobial Multi-lumen Central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is labeled in part: LIST NO. 43449 Recalled by Hospira Inc. Due to...
The Issue: Hospira has recieved reports that the vacuum needed to create suction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT and Brilliance iCT SP These systems are intended Recalled by...
The Issue: An artifact that resembles thrombus may appear on the image.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.