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. 2,535 recalls have been distributed to Indiana in the last 12 months.
Showing 32681–32700 of 53,528 recalls
Recalled Item: LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5...
The Issue: A portion of this lot of blood collection tubes was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morning Life Recalled by Won Industry Co. Due to Distribution of unapproved...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway Recalled by...
The Issue: Labeling error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compressible Limb Therapy System (Leg Cuffs Recalled by Won Industry Co. Due...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterFuse Tail Traction Tool Recalled by Vertebral Technologies, Inc. Due to...
The Issue: Fit issues have been identified with the Tail Traction Tool (PN 9116) when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LIFEPAK 1000 defibrillator is intended for use by personnel Recalled by...
The Issue: The firm has received complaints that the LIFEPAK 1000 Defibrillator is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICTSWEET(R) FARMS Recalled by The Pictsweet Company Due to Product may...
The Issue: Product may contain glass fragments
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GrebSet Micro-Introducer Kit Recalled by Vascular Solutions, Inc. Due to...
The Issue: Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System Recalled by Carestream Health...
The Issue: The firm received a complaint alleging that a DRX Revolution System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is a potential for radio frequency (RF) interference to alter wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor Recalled by Physio-Control, Inc. Due to The firm has...
The Issue: The firm has become aware of a potential device issue where the LIFEPAK 15...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Actavis Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product is out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg Recalled by Sun...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...
The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscopy Pack (1184) Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration full Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Software error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...
The Issue: Firm received a complaint of the tip holder breaking during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Open Procedure Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasal Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.