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. 1,084 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,084 in last 12 months

Showing 16141–16160 of 52,535 recalls

DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Vecuronium Bromide for Injection 10 mg Recalled by Teva Pharmaceuticals USA...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Ethosuximide Oral Solution USP 250 mg/5 mL Recalled by PAI Holdings, LLC....

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Cimetidine Hydrochloride Oral Solution 300 mg/5 mL Recalled by PAI Holdings,...

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin BIOLOX Delta Mod Head Recalled by Corin Ltd Due to The packaging...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek SmartView Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity-i Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Liner ECIMA Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Dual Mobility Recalled by Corin Ltd Due to The packaging...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Beckman Coulter Inc.

Recalled Item: Power Processor 3K Recalled by Beckman Coulter Inc. Due to Missing splash...

The Issue: Missing splash guard which may expose users to hazardous materials. .

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Screw Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing