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. 1,890 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,890 in last 12 months

Showing 2704127060 of 29,298 recalls

Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· GE Healthcare, LLC

Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Edwards Lifesciences, LLC

Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...

The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems...

The Issue: It has been confirmed from in-house testing that Direct Bilirubin (DBIL),...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zeego x-ray Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens issued a customer safety notice about the overlay of system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Endologix Inc

Recalled Item: Brand Name: AFX" Introducer System Recalled by Endologix Inc Due to...

The Issue: Endologix, Inc. initiated this voluntary recall of certain lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2013· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister...

The Issue: Ethicon Endo-Surgery is initiating a voluntary worldwide recall for ECHELON...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Life Technologies Corporation

Recalled Item: HSV 2 Primers Recalled by Life Technologies Corporation Due to Firm received...

The Issue: Firm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· ErgoSafe Product LLC dba Prism Medical Services

Recalled Item: 400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 Recalled by...

The Issue: MedCare Products has determined that a number of their Floor Lifts...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo(R) Lab Data Manager - Version VA11B and VA12A Systems Recalled by...

The Issue: Under certain conditions the system may not perform as intended, causing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Rauland-Borg Corp

Recalled Item: Responder 5 is a nurse call communication system that connects Recalled by...

The Issue: A counterfeited electronic component was identified in the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510613 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510613 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510121 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510076 Disposable Dual Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510180 Disposable Single Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510450 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: Dimension EXL LOCI Module TSHL Flex Reagent Cartridge (). Recalled by...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· SpineFrontier, Inc.

Recalled Item: Invue Split Driver Recalled by SpineFrontier, Inc. Due to Device design.

The Issue: Device design.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing