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. 1,945 recalls have been distributed to Missouri in the last 12 months.
Showing 17861–17880 of 29,298 recalls
Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...
The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...
The Issue: Replacement campaign on all units that have a gas spring head in aluminum.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Medical Charged-Particle Radiation Therapy System Recalled by Elekta,...
The Issue: The table shift in the vertical direction was inverted during the use of CMA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye Recalled by Alcon Research, Ltd. Due to Some ORA...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SQ-RX 1010 Pulse Generator Recalled by Boston Scientific Corporation Due to...
The Issue: The device can deliver an atypical amount of energy due to memory corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.