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. 933 recalls have been distributed to Oklahoma in the last 12 months.
Showing 48421–48440 of 49,976 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...
The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...
The Issue: The seat could break as a result of damage resulting from a seat belt being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...
The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precise Digital Accelerator Delivery of radiation to defined target volumes...
The Issue: There have been a small number of instances in hospitals where the joint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare¿ I-Fit" Shower Chair (Models 9780 Recalled by Invacare Corporation...
The Issue: On August 6, 2012, Invacare voluntarily recalled the Invacare¿ I-Fit" Shower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....
The Issue: During the manufacturing of the affected lot a manufacturing error has led...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic...
The Issue: There is a possibility that the ISKD limb lengthener may stop distracting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dippin' Stix Sliced Apples & Caramel with Peanuts Recalled by Reichel Foods,...
The Issue: Reichel Foods is recalling these products because the sliced apples have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Apple Slices & Fat Free Caramel Dip contained in the Recalled by Reichel...
The Issue: Reichel Foods is recalling these products because the sliced apples have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 LAS PN 0000280030 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien)...
The Issue: Potential failure of HALO Energy Generator to enter "stand by" mode when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 CTS PN 0000280050 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP (Base) PN 0000280000 ACL TOP is Recalled...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.