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. 2,609 recalls have been distributed to Oregon in the last 12 months.
Showing 13001–13020 of 28,488 recalls
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft Recalled by Ethicon...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Component for Laser Scanning Microscopes (LSM 700 Recalled by Zeiss, Carl...
The Issue: When the user tilts the transmitted light arm of the microscope to the end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starburst Talon Semi-Flex Electrosurgical Device Recalled by Angiodynamics...
The Issue: The devices are not labelled correctly. End users impacted by this issue may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4mm x 2.5 Fluted Pin Pouch Recalled by Exactech, Inc. Due to Potential for...
The Issue: Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega...
The Issue: There is a potential for the screws to have become loosened during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Recalled by...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. X-Port isp M.R.I Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.