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. 2,499 recalls have been distributed to Oregon in the last 12 months.
Showing 19941–19960 of 28,488 recalls
Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynasty Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom 2.8 implants Sterile The Axiom REG implants are used Recalled by...
The Issue: Following a FDA inspection showing that the firm failed to validate the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom REG implants Sterile The Axiom REG implants are used Recalled by...
The Issue: Following a FDA inspection showing that the firm failed to validate the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible that that the selected Plan-of-the Day could be accidently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba Mindray...
The Issue: Potential for a leak to occur on the back-up O2 and air e-size cylinder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter Recalled by Smith...
The Issue: The device could be subject to breaches of its sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-000VF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Recalled by...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volker 2080 Recalled by Hill-Rom, Inc. Due to The current construction of...
The Issue: The current construction of the side rail latch may not be able to support...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.