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. 2,831 recalls have been distributed to Georgia in the last 12 months.
Showing 5681–5700 of 29,505 recalls
Recalled Item: RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number:...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. W/O CDX BLUESTAR Recalled by Fresenius Medical Care Holdings,...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis SYS Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. W/O CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T GEN 2 Bibag without CDX Recalled by Fresenius Medical Care Holdings,...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to When global...
The Issue: When global edit is used to update multiple formulary properties...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX BLUESTAR Recalled by Fresenius Medical Care Holdings, Inc....
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Go Standard Carts Ref: (H45181VC and H45103VCW) Recalled by GE MEDICAL...
The Issue: Some Venue Go Standard Carts can develop an internal failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meera Mobile Operating Table-to support and position the patient immediately...
The Issue: Under certain conditions, an issue might prevent the device from performing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAZOR X robotic guidance system Recalled by Mazor Robotics Ltd Due to...
The Issue: Software update
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use Recalled...
The Issue: Skin grafts thin and non-uniform when using the affected blades. The issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethos Collar Stem Recalled by Onkos Surgical, Inc. Due to Potential for...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Male-Female Midsection with the following sizes and model numbers. a....
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.