Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,741 recalls have been distributed to Indiana in the last 12 months.
Showing 5661–5680 of 29,228 recalls
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: Brand Name: The Guardian System Product Name: The Guardian Model/Catalog...
The Issue: Device reaching End of Service prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solea Models 2.0 and 3.0 Laser Surgical Instrument Recalled by Convergent...
The Issue: It has been found that potential unintended laser activation can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAVH Recalled by American Contract Systems, Inc. Due to During an internal...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotics Pack SAH Recalled by American Contract Systems, Inc. Due to During...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotics Pack Recalled by American Contract Systems, Inc. Due to During an...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasc. Open CVOR SJH Recalled by American Contract Systems, Inc. Due to...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS PCSU SJH Recalled by American Contract Systems, Inc. Due to During an...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Heart SJH Recalled by American Contract Systems, Inc. Due to...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cath Cardiac Pack Recalled by American Contract Systems, Inc. Due to During...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sub Q Recorder Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.