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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,431 in last 12 months

Showing 3822138240 of 49,976 recalls

Medical DeviceMay 26, 2015· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb SofPort Advanced Optics Aspheric Lens Recalled by Bausch &...

The Issue: Haptics breaking during lens loading and insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2015· Smiths Medical ASD, Inc.

Recalled Item: CADD¿- Solis Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....

The Issue: Smiths Medical has become aware of an issue with an intermittent occurrence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2015· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: Recalled by...

The Issue: Haptics breaking during lens loading and insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: There exists a possible position sensor fault in the swivel base axis not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 0702-001-350Q Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Stryker Instruments is initiating a recall of the Neptune 2 Waste Management...

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

Class II — Potential Health HazardOngoing
FoodMay 22, 2015· Falcon Trading Co., Inc.

Recalled Item: Conventional Desiccated Coconut - Medium Shred 25 lb. bags. Exp Recalled by...

The Issue: Firm noticed stainless steel wire fragments, approximately .2 MM in diameter...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2015· Falcon Trading Co., Inc.

Recalled Item: Sunridge Candy-Coconut Chews Recalled by Falcon Trading Co., Inc. Due to...

The Issue: Firm noticed stainless steel wire fragments, approximately .2 MM in diameter...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2015· Vitamin Cottage Natural Food Markets, Inc.

Recalled Item: Natural Grocers Raw Macadamia Nuts Recalled by Vitamin Cottage Natural Food...

The Issue: Vitamin Cottage Natural Food Markets Inc. is recalling various lots of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications; exceeded specification at the 9 hour time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications; exceeded specification at the 9 hour time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2015· Takeda Pharmaceuticals North America, Inc.

Recalled Item: CONTRAVE (naltrexone HCl and bupropion HCl )extended-release tablets...

The Issue: Failed Tablet/Capsule Specifications: Potential tablet defect of broken...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2015· Medtech Products, Inc.

Recalled Item: SUCRETS Sore Throat & Cough Vapor Cherry lozenges Recalled by Medtech...

The Issue: Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 21, 2015· Exactech, Inc.

Recalled Item: Exactech Single Barrel Drill Guides The Single Barrel Drill Guide Recalled...

The Issue: Shipped to a single consignee prior to completion of final inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Elekta, Inc.

Recalled Item: Oncentra Brachy radiation therapy planning software designed to analyze and...

The Issue: Incorrect dose calculation for Regions of Interest (ROIs) defined on a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Exactech, Inc.

Recalled Item: Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical...

The Issue: Shipped to a single consignee prior to completion of final inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Healthcare Diagnostics Dimension Vista Systems Recalled by Siemens...

The Issue: Two software issues may occur in Vista software version 3.6.1. Issue #1:...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for...

The Issue: Bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Northern Digital Inc.

Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...

The Issue: Inadequate curing of adhesive, which may cause the two halves of the spheres...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· CooperSurgical, Inc.

Recalled Item: MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80 Recalled by CooperSurgical,...

The Issue: A diaphragm size 80 labeled box was incorrectly packaged with a size 85.

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

Class II — Potential Health HazardOngoing
DrugMay 20, 2015· Mylan Lab Inc

Recalled Item: Mycophenolic Acid Delayed-release Tablets Recalled by Mylan Lab Inc Due to...

The Issue: Failed Dissolution Specifications: Low out of specification dissolution results.

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

Class II — Potential Health HazardOngoing
Refund