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. 2,696 recalls have been distributed to Indiana in the last 12 months.
Showing 13241–13260 of 29,228 recalls
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for...
The Issue: Power supply (Model Number: TLC-2003) ME90A2403F01 (24 VDC, 3.75 A, 90 W, 1%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602...
The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 Recalled...
The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software Version (IUO) 5.4 Catalog Number: A31774 Recalled...
The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software Version 5.6.4 Catalog Number:A33178 OEM Customer...
The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to SOMATOM...
The Issue: SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for calibration error resulting in QC failures after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...
The Issue: The firm has become aware there is a potential problem with its DABRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/wing 5700LAX...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.