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. 2,711 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,711 in last 12 months

Showing 33013320 of 29,298 recalls

Medical DeviceJuly 26, 2024· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Recalled by...

The Issue: Reports have been received regarding open seals on the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Carbon Medical Technologies, Inc.

Recalled Item: BiomarC EX Fiducial Marker System Recalled by Carbon Medical Technologies,...

The Issue: This recall has been initiated due to a failure to provide an MRI Insert...

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

Class III — Low RiskOngoing
Medical DeviceJuly 26, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by Siemens...

The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by...

The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM CA 19-9 (250 Test - REF)-In vitro diagnostic Recalled by Siemens...

The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CA 19-9 (250 Test)-In vitro diagnostic use in Recalled by...

The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM CA 19-9 (250 Test)- In vitro diagnostic use Recalled by Siemens...

The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing