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 18421–18440 of 29,298 recalls
Recalled Item: Pacific Hemostasis FDP Latex Reagent Recalled by Fisher Diagnostics Due to...
The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lightspeed RT16 X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neusoft Medical NeuViz 64 Multi-slice CT Scanner System Recalled by Neusoft...
The Issue: Software defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare BrightSpeed X-ray system Recalled by GE Healthcare, LLC Due to...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery NM/CT 570c X-ray system Recalled by GE Healthcare,...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare lnnova IGS 540 ACT X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neusoft NeuViz 128 Multi-slice CT Scanner System Product Usage: The Recalled...
The Issue: Software defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery NM/CT 670. 670 Pro Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may...
The Issue: Packaging breach may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...
The Issue: Potential for electric shock in the case of a failure to install the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...
The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...
The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....
The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo MR355 Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...
The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.