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 25421–25440 of 28,654 recalls
Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreaCore¿ software. Versions subject to the limitation: 6.0 Recalled by...
The Issue: Vital Images, Inc. has found an issue in VitreaCore software though internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive has identified that the metalized coating on the IS3000 HD lamp...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...
The Issue: A Hand Piece high deployment force exceeded the maximum specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...
The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle" Recalled by Intra Pump...
The Issue: Product has the potential to have a clear debris on the tip of the needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterrad 100NX Recalled by Advanced Sterilization Products Due to Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the Sterrad 100NX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile...
The Issue: The firm discovered that unlatching can occur when overloaded transfer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare qube Compact Patient Monitor Recalled by Spacelabs...
The Issue: Spacelabs Healthcare qube Compact Patient Monitor, Model 91390, may fail to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System Recalled by Philips Medical Systems North America...
The Issue: A problem has been detected with Philips Model EPIQ 7 Ultrasound System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 2 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biotene Moisturizing Mouth Spray Recalled by GlaxoSmithKline, LLC. Due to...
The Issue: Label indicates, "Sweetened with xylitol and Sorbitol", however product does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Na+ Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.