Missouri Recalls
5,896 recalls on record affecting Missouri
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model Numbe
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore remained in service. More specifically, drops or jarring on a hard surface can cause the touchscreen input cable to loosen, resulting in unintended touchscreen behavior on the LVP, including random screen touches and/or lack of screen responsiveness to user input. Under the reported failure condition, unintended touch inputs may register at arbitrary screen locations without user interaction. These inputs occur intermittently and without a predictable pattern.
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Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.
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The Coffee Connexion Co., Inc recalls Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag a
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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The Coffee Connexion Co., Inc recalls Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag an
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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The Coffee Connexion Co., Inc recalls 1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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The Coffee Connexion Co., Inc recalls Aramark Cheese Sauce New & Improved, 25 lb., packaged in a t
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc
Due to stain present on the surface of affected foley catheters.
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Llorens Pharmaceuticals International Division, Inc. recalls Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement
Foreign object: black particulate matter
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Pork King Good, LLC recalls Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (
Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.
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Givaudan Flavors Corp recalls Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50
Product has the potential to be contaminated with Salmonella.
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AVID Medical, Inc. recalls Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UI
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75AM.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WA
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75-01.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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Ventec Life Systems, Inc. recalls VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, R
Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could occur that may lead to reduced below intended levels of fraction of inspired oxygen delivery prior to and during ventilation and this oxygen-enriched environment may increase fire risk
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Showing 20 of 5,896 recalls. Use search to filter further.