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. 1,091 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,091 in last 12 months

Showing 13801–13820 of 28,488 recalls

Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: Replacement ECG leadwires with snap ends REF/Catalog Number Description...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· GE Healthcare, LLC

Recalled Item: ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire...

The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· Cardiocommand Inc.

Recalled Item: CardioCommand Recalled by Cardiocommand Inc. Due to Possible corrosion of...

The Issue: Possible corrosion of the battery contact(s).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 10, 2019· Cadence Science, Inc.

Recalled Item: Cadence Science Pressure Control Glass Syringe Recalled by Cadence Science,...

The Issue: The glass syringe used with Pressure Control Syringes may potentially break...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2019· I.T.S. GmbH

Recalled Item: Rim Plate Recalled by I.T.S. GmbH Due to The titanium implant has the wrong...

The Issue: The titanium implant has the wrong article number laser marked on it.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2019· Xhale Assurance, Inc.

Recalled Item: Nasal Alar SpO2 Sensor Recalled by Xhale Assurance, Inc. Due to These...

The Issue: These Instructions for Use has missing instructions related to the checking...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· Qiagen Sciences, Inc.

Recalled Item: RNeasy DSP FFPE Kit (48) Recalled by Qiagen Sciences, Inc. Due to The...

The Issue: The deparaffinization solution contains a contaminant, which leads to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· Becton Dickinson & Company

Recalled Item: Alaris Pump Infusion Set Recalled by Becton Dickinson & Company Due to An...

The Issue: An incomplete occlusion can be caused by a variation in the wall thickness...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 6, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part Recalled by...

The Issue: User may suffer an electric shock when coming in contact with the exposed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· NeuroLogica Corporation

Recalled Item: Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The Recalled...

The Issue: Potential issue related to the operation of the safety latch within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2019· Monarch Medical Technologies

Recalled Item: Monarch Medical Technologies EndoTool IV Recalled by Monarch Medical...

The Issue: Insulin dosing calculations were erroneously high.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2019· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...

The Issue: Users with Android OS 8.0 and above may be unable to transfer values...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2019· XTANT MEDICAL INC

Recalled Item: OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe...

The Issue: The firm received one customer complaint concerning three OsteoSelect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer (reloadable) [9 pcs] - Product Usage: Is Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Oakworks Inc

Recalled Item: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401 Recalled by Oakworks Inc Due...

The Issue: Table assembly error with incorrect actuators for the lateral and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Neonatal Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Standard Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing