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. 2,641 recalls have been distributed to Oregon in the last 12 months.
Showing 8141–8160 of 28,488 recalls
Recalled Item: ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version...
The Issue: Due to interference with the Live Listen feature of hearing aid or AirPods,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PX200 Emergency Relief Bed Recalled by Oakworks Inc Due to Product label was...
The Issue: Product label was printed without the UDI number and warning label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oakworks Bed (Emergency Field Bed) Recalled by Oakworks Inc Due to The...
The Issue: The warning label was printed with the incorrect weight capacity. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 Liters Drain Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Recalled by Baxter Healthcare Corporation Due to Certain Peritoneal...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APD Drain Manifold Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Cap for PD Catheter Adapter Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Prong Manifold Set (with Luer Connectors) Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Effluent Sample Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus235- Proton Therapy System: to produce and deliver a proton Recalled...
The Issue: First layer of Uniform Scanning treatment fields is sometimes irradiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The C304-HIS device features a guide wire to access the vein Recalled by...
The Issue: The firm's internal processes identified that certain lots may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System Recalled by...
The Issue: Firm detected an increase in complaints related to fractured jaw tips of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: TEG5000 Analyzer (07-022 Recalled by Haemonetics Corporation...
The Issue: When the TEG 5000 Analyzer including TEG Analytical Software is used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 Recalled...
The Issue: It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Models: 3500 Recalled by Smiths Medical ASD Inc. Due...
The Issue: Multiple issues with the potential for interruption of therapy or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Model: Model 4000-0100-50 Recalled by Smiths Medical...
The Issue: Multiple issues with the potential for interruption of therapy or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement back up batteries distributed on or after April 1 Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Ventilators labeled as the following: a. Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: progenamatrix Human Keratin Matrix Recalled by ProgenaCare Due to Inner...
The Issue: Inner pouch seal may be inadequate resulting in lack of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Devices...
The Issue: Devices were subject to unapproved rework processes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.