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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 30461–30480 of 49,976 recalls
Recalled Item: GP161R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR GHIATAS Beaded Breast Localization Wire Recalled by Bard Peripheral...
The Issue: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: hCG Body Shaper Recalled by Gary Wood Due to Marketed without an Approved...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis has found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Taro Pharmaceuticals...
The Issue: Failed Content Uniformity Specifications; out-of-specification (OOS) results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PrednisoLONE Oral Solution USP Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LaBri's Body Health Atomic Recalled by Envy Me Due to Undeclared Sibutramine
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...
The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast...
The Issue: Missing Dome Pack accessory.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: French's Crispy Jalapenos Net Wt. 5 oz. (141.7g) Recalled by The French's...
The Issue: Product may contain foreign objects: rocks and metal fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.