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. 1,040 recalls have been distributed to Missouri in the last 12 months.
Showing 19661–19680 of 52,570 recalls
Recalled Item: Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software...
The Issue: Menu selections for users to access the oxygen (O2) sensor calibration were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...
The Issue: Reports have been received about the transcutaneous monitoring system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pure Dent¿ B700 Food Corn Starch packaged in 50 lb bags Recalled by Grain...
The Issue: A customer reported the presences of metal slivers ranging in length between...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mesalamine Delayed-Release Tablets Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Dissolution Specifications: Low out of specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL GROCERS ALMOND CLUSTERS DK CHOCOLATE NON-GMO Recalled by Vitamin...
The Issue: Undeclared peanut and milk allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO Recalled by Vitamin...
The Issue: Undeclared almond and milk allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...
The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Firefly Floorsitter Recalled by James Leckey Design Ltd Due to The firm...
The Issue: The firm received reports of a number of broken latches on the floorsitter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chemistry QC Premium Plus Recalled by Randox Laboratories Ltd. Due to The...
The Issue: The control target and range value for Sodium using the ISE indirect method...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Tests returning incorrect...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Tablets USP Recalled by Strides Pharma...
The Issue: Failed Tablet/Capsules Specifications: Oversized tablets were found in one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS....
The Issue: Embolization device delivery system may fracture at the distal section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.