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. 2,010 recalls have been distributed to Missouri in the last 12 months.
Showing 13581–13600 of 29,298 recalls
Recalled Item: Kit BD Max ExK DNA 2 USA Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Bacterial Panel EU Recalled by Becton Dickinson & Co. Due...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max MRSA XT Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukushima suction tubes Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: There was incorrect raw material used in the production of the identified lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The...
The Issue: Non-conforming devices are identified, which may not have been included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 05031656160 Recalled by Roche...
The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 07251670190 Recalled by Roche...
The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion systems with software version R1.2 -Interventional...
The Issue: The cold restart of Azurion R1.2 systems may take up to 7 minutes if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage:...
The Issue: Negative Bias with Lot EA9227.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Cogent Hemodynamic Monitoring System Recalled by ICU Medical,...
The Issue: Firm identified several software issues through internal testing of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom Receiver Recalled by Dexcom Inc Due to It has been reported that use...
The Issue: It has been reported that use of the mobile receiver with software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an in vitro diagnostic product intended for use Recalled by Randox...
The Issue: Randox Laboratories realigned RX Analyser Series calibration targets by 10%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Pelvic Trainer (MPT) Recalled by Ralston Group Due to The device was...
The Issue: The device was incorrectly listed with the FDA and is therefore considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to Potential...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186 Recalled by B....
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114 Recalled by B....
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187 Recalled by B....
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18TKSTN CONT EPID W/SOFT TIP NRFIT Catalog # 339191 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.