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. 2,877 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,877 in last 12 months

Showing 49815000 of 29,093 recalls

Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· NeuroLogica Corporation

Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...

The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· MRP, LLC dba Aquabiliti

Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...

The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: New warnings are being added to the Instructions for Use for all affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: IFU has been updated to include warnings about the risk of the inlet...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 27, 2023· TruAbutment Inc.

Recalled Item: Brand Name: TruScan Body Recalled by TruAbutment Inc. Due to Retroactive:...

The Issue: Retroactive: Due to defect and quality issues dental scanner may not scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2023· GE Medical Systems, SCS

Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...

The Issue: X-ray exposure termination audible signal on Senographe Pristina with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2023· Ossur H / F

Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...

The Issue: Knee batteries may need replacement with conforming batteries to ensure...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing