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.

52,570 total recalls
1,945 in last 12 months

Showing 1668116700 of 29,298 recalls

Medical DeviceMarch 28, 2018· Draegar Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...

The Issue: Software anomaly resulting in the loss of patient settings and stored...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips Ingenuity Core 728321 Recalled by Philips Medical Systems...

The Issue: A problem has been detected in the X-Ray Tube. The affected tubes have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT 882442 Recalled by Philips Medical Systems (Cleveland)...

The Issue: A problem has been detected in the X-Ray Tube. The affected tubes have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Teleflex Medical Europe Ltd

Recalled Item: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port Recalled...

The Issue: These one-way valves may disconnect at the joint between the two components...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use...

The Issue: Urea Nitrogen reagent kit demonstrated an increased incidence of Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Trilliant Surgical Ltd.

Recalled Item: Ratcheting Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due...

The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.Via VB20A model 1049610 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Functionality in the report sections "Findings Information" and "Summary of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Trilliant Surgical Ltd.

Recalled Item: Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due to Firm is...

The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: 708033 URODiagnost As a multifunctional universal imaging application system...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDiagnost Eleva 708036 As a multifunctional universal imaging...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDim Eleva 708032 As a multifunctional universal imaging application...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing