Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 2670126720 of 27,655 recalls

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· 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· 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· 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
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Irrigation Catheters (Models IRR-XXX-XX): 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
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· 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· 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· 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· 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 8, 2012· Parks Medical Electronics, Inc

Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...

The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...

The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...

The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....

The Issue: During the manufacturing of the affected lot a manufacturing error has led...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Diamedix Corporation

Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...

The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...

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

Class II — Potential Health HazardOngoing