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. 2,727 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,727 in last 12 months

Showing 2010120120 of 29,093 recalls

Medical DeviceAugust 25, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm received multiple reports of Xhibit Telemetry System going offline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· Sorin Group USA, Inc.

Recalled Item: St¿ckert S5 System Recalled by Sorin Group USA, Inc. Due to Sorin/LivaNova...

The Issue: Sorin/LivaNova is initiating a field correction on the S5 Heart-lung machine...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE/IMMULITE 2000 Systems Rubella IgM (RUM) Recalled by Siemens...

The Issue: Siemens received multiple customer complaints indicating an increase in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM) Recalled by Siemens...

The Issue: Siemens received multiple customer complaints indicating an increase in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· ICU Medical, Inc.

Recalled Item: Tego Connector Recalled by ICU Medical, Inc. Due to ICU Medical Inc. has...

The Issue: ICU Medical Inc. has identified a potential risk of leaking with certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Teleflex Medical

Recalled Item: WECK¿ Horizon" Manual-Load Ligating Clip Applier Recalled by Teleflex...

The Issue: Misbranded: Incorrect etching on the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Azer Scientific, Inc.

Recalled Item: Fruit Punch Glucose Recalled by Azer Scientific, Inc. Due to Out of...

The Issue: Out of Specification Microbiological test results

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra Cranial Access Kits Recalled by Integra LifeSciences Corp. d.b.a....

The Issue: Integra LifeSciences has been notified of a medical device recall by...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Baxter Corporation Englewood

Recalled Item: 0.2 Micron Filter Recalled by Baxter Corporation Englewood Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for all...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2016· Azer Scientific, Inc.

Recalled Item: Glucose Tolerance Beverage- Orange 50 gram Concentration Recalled by Azer...

The Issue: Out of Specification Microbiological test results

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· R & D Systems, Inc.

Recalled Item: R&D Systems Recalled by R & D Systems, Inc. Due to R&D Systems, Inc....

The Issue: R&D Systems, Inc. received two customer complaints that results of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integral Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Ventricular Catheter Accessory Kit Recalled by Integra LifeSciences...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing