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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,468 in last 12 months

Showing 3116131180 of 49,976 recalls

DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Potassium Chloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: Leakage of unit dose cups that may occur at the seal.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Metoclopramide Oral Solution Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 18, 2017· D. F. Stauffer Biscuit Co, Inc.

Recalled Item: FRONT: Stauffer's Animal Crackers Original Recalled by D. F. Stauffer...

The Issue: D. F. Stauffer Biscuit Co., Inc. is voluntarily recalling one specific best...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2017· Argon Medical Devices, Inc

Recalled Item: HARVEST NEEDLE 15GA X 2 Intended for the purpose of Recalled by Argon...

The Issue: The recalling firm received a complaint from one of their customers of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Argon Medical Devices, Inc

Recalled Item: BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G Recalled by Argon...

The Issue: The recalling firm received a complaint from one of their customers of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Argon Medical Devices, Inc

Recalled Item: T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN Recalled by Argon Medical...

The Issue: The recalling firm received a complaint from one of their customers of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance 64 System Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· BioMerieux SA

Recalled Item: ETEST XM256 (Cefuroxime) Recalled by BioMerieux SA Due to Potential...

The Issue: Potential performance issues. False Susceptible result instead of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance iCT SP X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing