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. 2,680 recalls have been distributed to Oklahoma in the last 12 months.
Showing 2581–2600 of 28,654 recalls
Recalled Item: Kirwan Surgical Products LLC Disposable 25-gauge bipolar pencil Recalled by...
The Issue: Potential for the outer stainless-steel tube to break or detach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to Due to a...
The Issue: Due to a software issue, automated dispensing cabinet devices may open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES 7 Drawer Auxiliary Tower Recalled by CareFusion 303,...
The Issue: Due to a software issue, automated dispensing cabinet devices may open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Due to a...
The Issue: Due to a software issue, automated dispensing cabinet devices may open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Recalled...
The Issue: Increase in complaints associated with a molding defect within the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aerin Medical VivAer Stylus Recalled by Aerin Medical, Inc. Due to Some...
The Issue: Some units in a single production lot were programmed incorrectly which will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST REPROCESSED BRUNS CURETTE #00 (BC00) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Flex reagent cartridge Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics is recalling two lots of their Dimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500) Recalled by MEDLINE INDUSTRIES, LP...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE MAGILL FORCEP (MAGF9) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O.R. SCISSORS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUMMELL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak seals...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE STRT KELLY HEMOSTAT (SK8039S) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST IUD REMOVAL HOOK 10" (504090) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1....
The Issue: Potential safety issues in Allura Xper R7.6- R8.1 systems where the Lifetime...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriALTIS TORQUE LIMITER Recalled by Gauthier Biomedical, Inc. Due to An out...
The Issue: An out of specification component may result in the device exhibiting torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...
The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...
The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Kits: 1) UROLOGY ROBOTIC PACK Recalled by Cardinal...
The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.