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 1641–1660 of 29,228 recalls
Recalled Item: The HemoCue Glucose 201 Microcuvettes are designed for use with Recalled by...
The Issue: Glucose microcuvettes experienced transit time outside of limits, so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Texium: 3 mL Recalled by BD SWITZERLAND SARL Due to Sterile, single use...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom One+ Continuous Glucose Monitoring System Recalled by Dexcom, Inc....
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G6 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope...
The Issue: The replacement rechargeable batteries inserted into the Welch Allyn...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model: Description/: MNA-420 ENC -H/K9303320 Recalled by Barco N.V. Due to...
The Issue: Cathode ray tube display system encoders and decoders have same MAC address;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...
The Issue: A software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog...
The Issue: a software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Recalled by Ortho-Clinical Diagnostics, Inc. Due to a...
The Issue: a software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name [REF]: Supply Server Recalled by CareFusion 303, Inc. Due to...
The Issue: During automated dispensing cabinet upgrade/installation/reimaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima Coil System /UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige Coil System /UDI-DI codes: PRES0153CXPPLT 00810068567311...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Product Name / UDI-DI code / Catalog No. Recalled by CareFusion...
The Issue: Antivirus software was not consistently installed on impacted devices during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GCE HEALTHCARE Zen-O lite Recalled by Ohio Medical Corporation Due to...
The Issue: Erroneous calibration values, potentially resulting in: as the device ages,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800WF Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SmartRelease ESTR (Endoscopic soft tissue release system)...
The Issue: Potential that the blade can unintentionally cut tissue prior to the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.