Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,378 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,378 in last 12 months

Showing 4840148420 of 49,976 recalls

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· 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· 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· 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· 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· 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· AGFA Corp.

Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...

The Issue: Loss of patient data can occur under certain circumstances due to...

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

Class II — Potential Health HazardOngoing
FoodAugust 8, 2012· American Importing Co, Inc

Recalled Item: Nature's Harvest Recalled by American Importing Co, Inc Due to Undeclared...

The Issue: Amport Foods is recalling one lot of pine nuts because there may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
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
DrugAugust 7, 2012· Mylan Pharmaceuticals Inc.

Recalled Item: Doxazosin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Cross...

The Issue: Cross Contamination w/Other Products: During stability testing...

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

Class II — Potential Health HazardOngoing
Refund