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. 2,544 recalls have been distributed to Oregon in the last 12 months.
Showing 18701–18720 of 28,488 recalls
Recalled Item: BrightView SPECT model number 882480 BrightView and BrightView X are...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...
The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT model number 882482 BrightView and BrightView X are Recalled...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...
The Issue: The bed exit alarm may not function properly if the alarm has been armed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...
The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5 Recalled by Carefusion 2200...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoracentesis/ Paracentesis Kit 10/CS Recalled by Carefusion 2200 Inc Due to...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP Recalled by Carefusion 2200 Inc Due...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manometer Recalled by Carefusion 2200 Inc Due to The integrity of the...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Internal Hex Healing Abutment Recalled by Ace Surgical Supply Co.,...
The Issue: Incorrect device was packaged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint - 3R Recalled by Siemens Medical Solutions USA Inc....
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090 Recalled by Signal...
The Issue: Potential for poly tip of the mallet to come off during use. Potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartTools Knee System Orthopedic Stereotaxic Instrument Recalled by...
The Issue: There has been an increase in the number of complaints regarding bent or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software updates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.