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. 2,619 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,619 in last 12 months

Showing 401420 of 52,535 recalls

DrugDecember 19, 2025· Novo Nordisk Inc.

Recalled Item: Wegovy (semaglutide) Injection Recalled by Novo Nordisk Inc. Due to Presence...

The Issue: Presence of Particulate Matter: Hair was found in a prefilled syringe

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: traZODONE Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA) Inc...

The Issue: Failed Tablet/Capsule Specifications: Product complaint received that some...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE TITAN 3T Model MRT-3010/MEXL-3010 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000F Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000H Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Altruan GmbH

Recalled Item: Wondfo Streptococcal A At-Home Self-Test. At-home test for group A Recalled...

The Issue: Product not cleared by the FDA.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Altruan GmbH

Recalled Item: Brand Name: Bisaf Strep A Self-Test. Test for detection of Recalled by...

The Issue: Product not cleared by the FDA.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

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

Class II — Potential Health HazardOngoing