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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.
Showing 23001–23020 of 28,654 recalls
Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...
The Issue: Possibility of image artifacts during data acquisition when using Adaptive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity Core 128. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 16 Surgical Skin Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence...
The Issue: Philips discovered that a software defect exists in marketed product wherein...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...
The Issue: Outer package product label incorrectly identifies the product as FiberOptix...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity Core. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DermaPen Pro Model Recalled by Derma Pen, LLC Due to Derma Pen initiated a...
The Issue: Derma Pen initiated a field communication for Dermapen after receiving an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse...
The Issue: Under certain circumstances the patient Demographics in a report exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Toothbrush Recalled by Norwex Usa Inc Due to The toothbrush head can...
The Issue: The toothbrush head can potentially disengage from the handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Inserter for Titanium Elastic Nails Recalled by Synthes, Inc. Due to...
The Issue: The Inserter has the potential for mechanical failures such as breakage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Allure BiPlane Series: Model 722013 Allura Xper FD20...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Xper cardio systems R7.6 Model : 722133 Product Recalled...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Xper vascular system Model : 722124 Product Usage:...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare INTEGRIS cardio system Model : 722121 Product Usage:...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.