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. 2,646 recalls have been distributed to Oregon in the last 12 months.
Showing 6661–6680 of 50,914 recalls
Recalled Item: Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9% Recalled by Brassica...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...
The Issue: Their is the potential that Universal Clip applier may not load clip after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...
The Issue: Their is the potential that Universal Clip applier may not load clip after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 SS/PD Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO Recalled by Angiodynamics,...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Recalled by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Due to...
The Issue: Due to capacitor manufacturing issue, their is a potential that Flat Panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embrace Drill Tower Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...
The Issue: The surgical techniques for the Embrace Shoulder Instruments -Drill Tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.