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. 2,496 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,496 in last 12 months

Showing 2386123880 of 49,976 recalls

Medical DeviceNovember 9, 2018· LivaNova USA

Recalled Item: Perfusion Pack Recalled by LivaNova USA Due to 4-way stopcocks and stopcock...

The Issue: 4-way stopcocks and stopcock manifold assembled in certain perfusion tubing...

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

Class II — Potential Health HazardOngoing
DrugNovember 9, 2018· AMERICAN HEALTH PACKAGING

Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by AMERICAN...

The Issue: Cross contamination with other products: This sub-recall is being initiated...

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

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2018· Ecolab Inc

Recalled Item: Equi-Soft Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...

The Issue: Labeling: Label mix-up - the label on the product may not match the formula...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2018· Ecolab Inc

Recalled Item: Medi-Stat Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...

The Issue: Labeling: Label mix-up - the label on the product may not match the formula...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2018· Konica Minolta Healthcare, Americas, Inc.

Recalled Item: Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17 Recalled...

The Issue: Unintentional U-Arm movement

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

Class II — Potential Health HazardOngoing
FoodNovember 8, 2018· Rich Products Corp

Recalled Item: VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 09076 / Recalled...

The Issue: Possible contamination with cleaning chemicals.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2018· Schwan's Global Supply Chain, Inc.

Recalled Item: Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz. Recalled by...

The Issue: One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 7, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: Stationary Fluoroscopic X-ray System CombiDiagnost R90 Recalled by Philips...

The Issue: kV/mA lockin not functioning as specified which may result in the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2018· Volcano Corporation

Recalled Item: Philips Volcano FFR software used in the following systems connected...

The Issue: Interoperability issue that affects certain systems that use the recalled...

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

Class II — Potential Health HazardOngoing
DrugNovember 7, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Clopidogrel Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specification: Out-of-Specification results were observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2018· L. Perrigo Company

Recalled Item: Antacid Tablets Recalled by L. Perrigo Company Due to Presence of foreign...

The Issue: Presence of foreign substance: Product found to contain metal particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2018· Breckenridge Pharmaceutical, Inc.

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Breckenridge Pharmaceutical,...

The Issue: Failed Stability Specifications: Out-of-Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS T2X table Recalled by Deerfield Imaging, Inc. Due to Table may drift...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 300 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 100 table Recalled by Deerfield Imaging, Inc. Due to Table may...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· COVIDIEN LLC

Recalled Item: 8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve)...

The Issue: The product was released into commercial distribution while subject to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Bausch & Lomb Surgical, Inc.

Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...

The Issue: Cosmetic imperfections on the surface of some lenses.

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

Class II — Potential Health HazardOngoing