Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,711 recalls have been distributed to Missouri in the last 12 months.
Showing 1641–1660 of 29,298 recalls
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: 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: 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: 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: 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: 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: 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.
Recalled Item: Brand Name: Valeda Light Delivery System Product Name: Light Based Recalled...
The Issue: U.S. customers were shipped devices that were configured for the European...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800W 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: Z-800F 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: DxI 9000 Access Immunoassay Analyzer C11137 Recalled by Beckman Coulter,...
The Issue: Analyzer has calibration issues where curves switched from passed to failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name:...
The Issue: Electrode placement labels on the Digital Acquisition Box (DAB) were applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.