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. 1,730 recalls have been distributed to Oregon in the last 12 months.
Showing 47221–47240 of 50,914 recalls
Recalled Item: Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product Usage:...
The Issue: Merit Medical Systems is recalling various lots of Performa Cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels...
The Issue: The product has the potential for false negative or delayed reaction for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptex* Latex D Recalled by Remel Inc Due to The product may give weak or...
The Issue: The product may give weak or false negative test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: california Pizza Kitchen crispy thin crust Recalled by Nestle USA, Inc -...
The Issue: Plastic contamination. Four pizzas with specific production codes, are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DiGiorno pizzeria Recalled by Nestle USA, Inc - Northbrook Pizza Head Office...
The Issue: Plastic contamination. Four pizzas with specific production codes, are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SexVoltz All Natural Herbal Supplement Recalled by Beamonstar Products Due...
The Issue: Marketed Without an Approved NDA/ANDA; products have been found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit Recalled by...
The Issue: cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Velextra All-Natural Herbal Supplement Recalled by Beamonstar Products Due...
The Issue: Marketed Without an Approved NDA/ANDA; products have been found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...
The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...
The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SafetyGlide Allergy. Sterile Allergy Treatment Syringe Tray. Recalled by...
The Issue: There has been an increase in complaints regarding the needle/safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...
The Issue: It is possible for an intermittent error to occur in the gantry sensor of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...
The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...
The Issue: Unexpected movement during beam delivery may not be detected if there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...
The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.