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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 561–580 of 53,528 recalls
Recalled Item: Allwell Angioplasty Pack /B Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Recalled...
The Issue: Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Recalled by...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abre Venous Self-Expanding Stent System Recalled by Medtronic Inc Due to...
The Issue: Stents may be impacted by a Nitinol anomaly which causes a reduced stent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S. Product Code (REF): 782108. MR systems with Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148 Recalled by Philips...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T. Product Code (REF): (1) 781342 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700. Product Code (REF): (1) 782120 Recalled by Philips North America...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X. Product Code (REF): (1) 781358 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with Recalled...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T. Product Code (REF): Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X. Product Code (REF): (1) 781356 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700. Product Code (REF): 782130. MR systems Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T. Product Code (REF): (1) 781341 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and...
The Issue: Complaints received that Vanta A71200 CP App does not function as intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter...
The Issue: Boston Scientific is initiating the removal of certain batches of Coyote"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.