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. 2,882 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,882 in last 12 months

Showing 39013920 of 52,535 recalls

Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE IRIS Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE BLAKE...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE CEMENT...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2024· Sklar Instruments

Recalled Item: ECONO STERILE medical procedure kits labeled as: ECONO STERILE IUD Recalled...

The Issue: Reports of various packaging issues that may result in a breach of the...

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2024· Grecian Delight/Kronos

Recalled Item: Nick The Greek Spicy Yogurt Pail Recalled by Grecian Delight/Kronos Due to...

The Issue: potential for salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2024· Grecian Delight/Kronos

Recalled Item: US Foods Chef's Line Greek Yogurt Tzatziki 4lbs tub Recalled by Grecian...

The Issue: potential for salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2024· Grecian Delight/Kronos

Recalled Item: Grecian Delight Tzatziki sauce Recalled by Grecian Delight/Kronos Due to...

The Issue: potential for salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 2, 2024· RemedyRepack Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by RemedyRepack Inc. Due to...

The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: X-Flow prostatectomy catheter Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemo software Recalled by A L I Technologies...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Accriva Diagnostics, Inc.

Recalled Item: VerifyNow P2Y12 Platelet Reactivity Test Recalled by Accriva Diagnostics,...

The Issue: Platelet Reactivity Test distributed without appropriate US-FDA market...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: McKesson Cardiology Hemo software Recalled by A L I Technologies Ltd Due to...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemodynamics software Recalled by A L I...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: Folysil Silicone Foley Catheters Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Moximed, Inc.

Recalled Item: MISHA Knee System Implant Small Recalled by Moximed, Inc. Due to Knee...

The Issue: Knee implant may fracture due to a supplier-related issue with one component...

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

Class II — Potential Health HazardOngoing
FoodNovember 27, 2024· Bazzini LLC

Recalled Item: NuGo Dark Chocolate Pretzel with Sea Salt Recalled by Bazzini LLC Due to...

The Issue: The product is being recalled because of undeclared milk .

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 27, 2024· Bazzini LLC

Recalled Item: NuGo Dark Pretzel/Chocolate Chip Multipack 18 ct. Recalled by Bazzini LLC...

The Issue: The product is being recalled because of undeclared milk .

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 27, 2024· Bazzini LLC

Recalled Item: NuGo Dark Chocolate Chip Recalled by Bazzini LLC Due to Undeclared Milk

The Issue: The product is being recalled because of undeclared milk .

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund