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. 2,660 recalls have been distributed to Oklahoma in the last 12 months.
Showing 5001–5020 of 28,654 recalls
Recalled Item: Terragene Integron IT26-C Terragene Integron IT26-C with extender Benco...
The Issue: Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator Recalled by...
The Issue: During internal review of Polaris battery assembly data from the HiPot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips North America Due to If the Patient...
The Issue: If the Patient Interface Monitor (PIM) Cable is plugged/unplugged frequently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Flo-Thru Intraluminal Shunt Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Floseal Hemostatic Matrix Fast Prep Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix NL Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Flo-Rester Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI-GUARD SUPPLE Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Coseal Premix Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (GLOBAL) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Preveleak Surgical Sealant Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Ostene Hemostasis Material Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix RECOTHROM Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella Connect Recalled by Abiomed, Inc. Due to The following features have...
The Issue: The following features have been disabled from the web-based portal because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.