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. 2,597 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,597 in last 12 months

Showing 11011120 of 29,093 recalls

Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Solution Set Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM Solution Set Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Northeast Scientific Inc.

Recalled Item: NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter....

The Issue: Potential for breaches in the sterile barrier packaging, compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Biograph mMR. Model Number: 10433372. Recalled by Siemens Medical Solutions...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Vantive US Healthcare LLC

Recalled Item: Sharesource Connectivity Platform for Use with Homechoice Claria Product...

The Issue: Vantive has identified a software defect within the Sharesource Claria...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Vida Fit. Model Number: 11410481. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot. Model Number: 10684333. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Lumina (DE). Model Number: 11344916. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma. Model Number: 10849582. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio. Model Number: 10276755. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing