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 6321–6340 of 50,914 recalls
Recalled Item: Ingenia 1.5T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYROSCAN T10-NT Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 3.0T Quasar Dual Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology Recalled...
The Issue: Product incorrectly labelled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranquility & Teachings William Monague plate set Recalled by Canadian Art...
The Issue: Product has been recalled because it may exceed FDA guidance levels for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses...
The Issue: System error messages may delay the ability to test patient samples and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...
The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...
The Issue: Due to a misaligned calibration of the wired controller that may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Full Length 070 Access System Recalled by ROUTE 92 MEDICAL...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical 070 Reperfusion System Recalled by ROUTE 92 MEDICAL INC Due...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.