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. 1,999 recalls have been distributed to Missouri in the last 12 months.
Showing 14661–14680 of 29,298 recalls
Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Malleable Recalled by Gyrus ACMI, Inc. Due to Olympus Diego...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Total Ankle Prosthesis Tray Recalled by Integra LifeSciences Corp....
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Total Ankle Prosthesis Tray Recalled by Integra LifeSciences Corp....
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Diego Elite Console MDCONS 100 Recalled by Gyrus ACMI, Inc. Due to...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Recalled by Integra LifeSciences Corp. Due to The Salto...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULRICH Torque Limiting Handle for use with a Set Screw Recalled by ulrich...
The Issue: Certain Torque Limiting Handles in the field are beyond their 3 year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25 Recalled by Becton...
The Issue: BD PAS received customer complaints indicating the absence of the bevel on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity ci-series System Control Module software version 2.5.1...
The Issue: Potential performance issues in the Alinity-ci software version 2.5.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to Potential...
The Issue: Increased risk of false positive Enterobacteriaceae and Escherichia coli...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...
The Issue: Elevated rates of false positive results for Campylobacter and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...
The Issue: When a patient is selected in the patient data and another patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBeam Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to...
The Issue: Certain lots may develop an internal leak due to a micro-crack in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled...
The Issue: Based on internal investigations, Fresenius Kabi has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRIdian Linac Radiation Therapy System Model 10000 and 20000 Recalled by...
The Issue: Issue with transferring treatment regiment from one system to another....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.