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. 1,077 recalls have been distributed to Indiana in the last 12 months.
Showing 16941–16960 of 53,528 recalls
Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progesterone Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg Recalled by Alvogen,...
The Issue: Subpotent drug: Out of specification for assay of naloxone and buprenorphine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: In-View Clear Leggings Bulk Non-Sterile Recalled by Cardinal Health 200, LLC...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-View Clear Leggings Sterile Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-View Clear Leggings Sterile Non-Sterile Recalled by Cardinal Health 200,...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Angiography Drape Bulk Non-Sterile Recalled by Cardinal Health 200,...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Angiography Drape Sterile Recalled by Cardinal Health 200, LLC Due...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit Therapeutics - Product Usage: intended for use Recalled...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit - Product Usage: intended for use in Recalled by Fenwal...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus MNC Apheresis Kit - Double Needle - Product Usage: Recalled by Fenwal...
The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Infusion Pump Module Recalled by BioMedical Equipment Service Co...
The Issue: Bezel repair parts used, not by the original manufacturer, to service and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Replacement Backflush Brush Needles (23 gauge/0.6mm)-for use in...
The Issue: Mislabeled: 1281.B1D Disposable Replacement Backflush Brush Needles label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems are advanced continuous-rotation computed tomography...
The Issue: Philips has internally detected an issue with the actuators used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Recalled by Arthrex, Inc. Due to The color indicator on the...
The Issue: The color indicator on the proximal end of the shaft of the AR-8770-02 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Midline Catheter Dressing Change Kit with Statlock - Product Usage: Recalled...
The Issue: Evidence of face masks or other material in the seal in several kits,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...
The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI Recalled by...
The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter...
The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...
The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.