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. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 27841–27860 of 28,488 recalls
Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...
The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....
The Issue: When using the EasyLink Quality Control Package the system may not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...
The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...
The Issue: There was an error on the outer labeling of this device. The inner label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...
The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantage Workstations Recalled by GE Healthcare, LLC Due to...
The Issue: GE Healthcare is informing you of incorrect measurements when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Seno Advantage 1.x Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has become aware of an issue associated with the magnification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...
The Issue: GE Healthcare has become aware of a potential safety issue due to incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...
The Issue: Philips is issuing a software update to the Intellispace Portal systems to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc...
The Issue: The recall was initiated because LMANA has received a complaint that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)...
The Issue: The Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical...
The Issue: On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal software and Extended Brillance Workspace software...
The Issue: The Intellispace Portal software and Extended Brillance Workspace software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 .019.038S...
The Issue: Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage Profiler SOB Panel PN 97300 Used for the Recalled by Alere San...
The Issue: Certain lots of the affected products may have significantly decreased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal software Product Usage: Intellispace Portal is a...
The Issue: In the Multi-Modality Tumor Tracking application, when changing the contours...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage BNP PN 98000XR Intended to be used as Recalled by Alere San...
The Issue: Certain lots of the affected products may have significantly decreased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.