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. 2,674 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,674 in last 12 months

Showing 2812128140 of 29,093 recalls

Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Recalled by...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Capsule Tech Inc.

Recalled Item: Capsule Neuron Docking Station Recalled by Capsule Tech Inc. Due to Capsule...

The Issue: Capsule Neuron Docking Station may experience a lost connection, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Control Set Recalled by...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Intact PINP Control Set Recalled by Immunodiagnostics Systems Ltd...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· AmeriWater Inc

Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...

The Issue: The firm was notified that a malfunction of the device was caused by an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Integra LifeSciences Corporation

Recalled Item: Integra CRW Precision Arc (CRWPRECISE) Recalled by Integra LifeSciences...

The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Integra LifeSciences Corporation

Recalled Item: Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by...

The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Intuitive Surgical, Inc.

Recalled Item: Tip Cover for 8mm Monopolar Curved Scissors (Hot Shears)Accessory Recalled...

The Issue: There is potential for the sterility of the product to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: Stryker MANTIS TORQUE WRENCH Manufactured by: Stryker pine Recalled by...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: Stryker XIA 3 TORQUE WRENCH Manufactured by: Stryker Recalled by Stryker...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Embolectomy Catheters (Models A44XX Recalled by Applied Medical Resources...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent...

The Issue: Firm has received complaints from customers of "Abnormal Reaction" errors...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Biliary Catheters (Models A47XX and CB0XXXXX): Model Numbers & Description:...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing