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. 2,678 recalls have been distributed to Missouri in the last 12 months.
Showing 6861–6880 of 29,298 recalls
Recalled Item: Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33...
The Issue: An unexpected shutdown of the IABP may occur due to loss of communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Hospital Electronics System (HES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: There have been reported failures of the high pressure helium regulator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Model Nos. 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85...
The Issue: An unexpected shutdown of the IABP may occur due to loss of communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Hoffmann LRF Recalled by Stryker GmbH Due to Stryker has identified...
The Issue: Stryker has identified a nonconformance in specific lots of Hoffmann LRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial mobile application Recalled by Securitas Healthcare LLC Due to The...
The Issue: The mobile application for Android devices downloaded from the Google Play...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA comprises AST Filters in conjunction with VITEK MS Recalled by...
The Issue: For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avanos Ballard Oral Care Swab Recalled by Avanos Medical, Inc. Due to...
The Issue: Incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE designed specifically for clinical use in the Recalled by...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE PRO-Analyzer designed specifically for clinical use in the...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE- Analyzer designed specifically for clinical use in the Recalled...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE PRO )-Analyzer designed specifically for clinical use in Recalled...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...
The Issue: Potential for product manifold to crack during use on patients, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...
The Issue: Potential for product manifold to crack during use on patients, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.