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 7761–7780 of 28,488 recalls
Recalled Item: Diasol Acid Concentrate 100 Recalled by Diasol, Inc Due to Due to labeling...
The Issue: Due to labeling issue. The box label is different that the gallon label in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute...
The Issue: (1)Software version 2.74 upgrade and (2)hardware related cause that affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco Medical Network Adapter Recalled by BARCO NV Due to installation issues
The Issue: installation issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORCA FOAM STANDARD CUBE 10x10x10 mm Recalled by GELITA MEDICAL GMBH Due to...
The Issue: In routine bioburden testing, higher than acceptable levels of Endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone Recalled...
The Issue: An incorrect sizing label was applied to the carton packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acidified Concentrate Distribution and Storage-The Isopure ACDS (Acidified...
The Issue: Acidified Concentrate Distribution System potential electrical safety hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT STAT Troponin-I Reagent Kit Recalled by Abbott Laboratories Due to...
The Issue: One lot of reagent was manufactured with insufficient quantities of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...
The Issue: Potential communication issue in which the Vanta Clinician Programmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...
The Issue: Potential for Vanta Clinician Programmer Application (CP App) A71200...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare N1 TiUltra TCC NP 3.5x13mm Recalled by Nobel Biocare Due to...
The Issue: Due to the presence of a burr which may cause an aspiration risk to patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5" Recalled by Stradis...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Scissors Iris Curved 4.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.