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. 1,937 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,937 in last 12 months

Showing 2122121240 of 29,298 recalls

Medical DeviceFebruary 26, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...

The Issue: Dialyzer header leak due to possible improper torque

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...

The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm has received one report of values for patient height and weight...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· Scottcare Corporation

Recalled Item: TeleSentry Battery Recalled by Scottcare Corporation Due to The firm...

The Issue: The firm received a complaint of the battery exploding while recharging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 74" (188cm) approximately 9.0ml Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 31" (79 cm) Appx. 3.4 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 110" (279 cm) Appx 13.8 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Diabetic Walker Product Usage: Rebound Diabetic Walkers are used...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Air Walker Product Usage: Rebound Air Walkers are indicated Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Angio WorkStation: XIDF-AWS801v6.00 Recalled...

The Issue: During a procedure the Peak Skin Dose (PSD) value was displayed on the DTS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader Custom Lite Product Usage: Unloader Custom Lite is an Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...

The Issue: After importing, the segmentation results appear mirrored at the CARTO...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Custom Product Usage: Rebound Cartilage Custom is an...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Papoose Infant Spine Immobilizer Item # Item Description: PA-100 Papoose...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing