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. 2,702 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,702 in last 12 months

Showing 2098121000 of 52,535 recalls

Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: US Clinical 20mL Programmable Pump. Catalog No. 01827 The device Recalled by...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 11827 The device is Recalled by...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Nikon Metrology

Recalled Item: Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225...

The Issue: The manufacturer identified a risk that their products might fail to comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Philips North America, LLC

Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...

The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Zimmer Biomet, Inc.

Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...

The Issue: Potential for the expiration date on the outer label that was applied by...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: Wave Prep Tubes (1710-03) and single use cups (17--00-24) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
DrugDecember 23, 2019· GSK Consumer Health, Inc

Recalled Item: Theraflu Cough Relief Recalled by GSK Consumer Health, Inc Due to Labeling:...

The Issue: Labeling: Label Lacks Warning: Product recalled due to absence of a warning...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 23, 2019· Reichel Foods Inc.

Recalled Item: Pro2Snax To The Max snack tray containing Sweet Gala Apples Recalled by...

The Issue: Products are being recalled due to Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 23, 2019· Reichel Foods Inc.

Recalled Item: Pro2Snax To The Max snack tray containing Sliced Apples Recalled by Reichel...

The Issue: Products are being recalled due to Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BUP 15MG/CLON 300MCG/ FENT 1500MCG/ML(40) INJ in 20 mL syringe Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: HYDROMORPHONE 3MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: TESTOSTERONE CYP 200MG/ML OIL INJ in 10 mL vial Assurance Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BUP 5MG/MORP 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund