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 7541–7560 of 28,488 recalls
Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...
The Issue: Due to increase in Li-Ion Battery failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...
The Issue: Detachment controller, of an aneurysm embolization system, has an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter...
The Issue: Product may not be sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium (Li) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...
The Issue: Retroactively reported correction from 2022: A software defect may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400 Recalled by...
The Issue: Blister package had an unsealed edge compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berkeley VC-10 Vacuum Curettage System Recalled by Olympus Corporation of...
The Issue: Update to the Instruction for Use (IFU): Olympus is adding a new warning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B. Braun CARESITE Port Access Kit w/Tegaderm Recalled by Medical Action...
The Issue: The kits were incorrectly labeled with an extended expiration date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESITE SMALLBORE EXT SET T-PORT 5 IN. Recalled by B. Braun Medical, Inc....
The Issue: The extension set has a high probability of potential failure which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRASITE US04TL Smallbore T-Port Extension Set Recalled by B. Braun...
The Issue: The extension set has a high probability of failure which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Tube Sodium Fluoride: 100 mg Recalled by Becton Dickinson &...
The Issue: The affected product contains isobutylene which has recently demonstrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Set Recalled by B. Braun Medical, Inc. Due to The extension set...
The Issue: The extension set has a high probability of failure which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male...
The Issue: Sterile extension sets were distributed without an expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to A part defect...
The Issue: A part defect with the wash 1 syringe of an SARS-CoV-2 assay could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.