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. 2,664 recalls have been distributed to Oklahoma in the last 12 months.
Showing 3741–3760 of 49,976 recalls
Recalled Item: Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Merlin PCS 3650 programmer Model 3330 The Merlin PCS Recalled by Abbott...
The Issue: Due to a programmer software anomaly, during finalizing of the leadless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685....
The Issue: A software bug within the Gen 2 StatStrip Hospital Meter firmware leads to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog...
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683....
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216 Recalled by...
The Issue: The following four issues are included: 1. Certain Channel Settings may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Subpotent and Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine DR Capsules USP 60 mg Recalled by Rising Pharma Holding, Inc. Due...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Rising Pharma Holding,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Rising Pharma Holding,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VACUETTE SAFELINK Recalled by Greiner Bio-One GmbH Due to The VACUETTE...
The Issue: The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duravent Silicone Ventilation Tube. Model Number: 240075. Recalled by...
The Issue: Potential that Duravent Silicone Ventilation Tubes may contain incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo USA, Inc. Due to...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.