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. 1,030 recalls have been distributed to Oklahoma in the last 12 months.
Showing 22301–22320 of 49,976 recalls
Recalled Item: Replacement ECG leadwires with snap ends REF/Catalog Number Description...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cadence Science Pressure Control Glass Syringe Recalled by Cadence Science,...
The Issue: The glass syringe used with Pressure Control Syringes may potentially break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioCommand Recalled by Cardiocommand Inc. Due to Possible corrosion of...
The Issue: Possible corrosion of the battery contact(s).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated...
The Issue: Reported complaints of cracks being observed, prior to use, on swivel wye...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA RF IgM Well Recalled by Phadia Ab Due to Potential for reporting low...
The Issue: Potential for reporting low assay results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leadwire sets with snap ends: REF/Catalog Number Description 2106381-001 ECG...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECG Trunk Cables: REF/Catalog Number Description 2106305-001 ECG Trunk Cable...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rim Plate Recalled by I.T.S. GmbH Due to The titanium implant has the wrong...
The Issue: The titanium implant has the wrong article number laser marked on it.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...
The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...
The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nasal Alar SpO2 Sensor Recalled by Xhale Assurance, Inc. Due to These...
The Issue: These Instructions for Use has missing instructions related to the checking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNeasy DSP FFPE Kit (48) Recalled by Qiagen Sciences, Inc. Due to The...
The Issue: The deparaffinization solution contains a contaminant, which leads to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Recalled by Becton Dickinson & Company Due to An...
The Issue: An incomplete occlusion can be caused by a variation in the wall thickness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The Recalled...
The Issue: Potential issue related to the operation of the safety latch within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part Recalled by...
The Issue: User may suffer an electric shock when coming in contact with the exposed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item FG 10106 Recalled by Barlean's Llc Due to Undeclared Sulfites
The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item FG 10146 Recalled by Barlean's Llc Due to Undeclared Sulfites
The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item FG 10149 Recalled by Barlean's Llc Due to Undeclared Sulfites
The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item FG 10089 Recalled by Barlean's Llc Due to Undeclared Sulfites
The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....
Recommended Action: Do not consume. Return to store for a refund or discard.