Product Recalls in Oregon
Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,470 recalls have been distributed to Oregon in the last 12 months.
Showing 24441–24460 of 28,488 recalls
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accell Evo3C Demineralized Bone Matrix Recalled by Integra LifeSciences...
The Issue: This lot of Accell Evo3C Demineralized Bone Matrix, 5cc was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerSys¿ Hip System Recalled by Zimmer, Inc. Due to During routine...
The Issue: During routine inspection, beaded hip stem forgings received from supplier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw...
The Issue: Small Bone Innovations (SBi) is recalling all lots of 3.0/4.0mm AutoFIX"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser...
The Issue: Laser Aperture label was not applied to certain GYC-1000 Green Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part...
The Issue: Alcon CUSTOM-PAK which is supposed to contain a 27G Anterior Chamber Cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Operative Cholangiogram Catheter Recalled by Teleflex Medical Due to...
The Issue: Several complaints were received for the metal support tube missing from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Resuscitator Bag Series: AF1000 Recalled by Ventlab LLC Due to The...
The Issue: The pop-off valve in the defective devices remain open and a squeeze of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...
The Issue: Surface finish is different than specified. The implant has 30 grit blast on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...
The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...
The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.