Product Recalls in Maryland

Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,898 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,898 in last 12 months

Showing 33413360 of 29,093 recalls

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
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