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. 2,590 recalls have been distributed to Oregon in the last 12 months.
Showing 14341–14360 of 28,488 recalls
Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Standard Base Recalled by Community Products, LLC Due to A...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Low Base Recalled by Community Products, LLC Due to A design...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton E-Pacer Recalled by Community Products, LLC Due to A design change to...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable Pump Recalled by Flowonix Medical Inc Due to The pump...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Clinician Programmer (Touchscreen) Software version 2.00.29...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmer (Grand Prime) Software version 2.00.29 Recalled by...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump Recalled by Flowonix Medical Inc Due to The...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump (Clinical) Recalled by Flowonix Medical Inc...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV1000 Clinical Platform Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Potential for an electrical short circuit leading to possible fire hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System 10 MM Recalled by Conmed Corporation...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System 15 MM Recalled by Conmed Corporation...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System" Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via syngo.CT Cardiac Function Recalled by Siemens Medical Solutions...
The Issue: There is a potential risk of a wrong measurement in the annulus plane during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via syngo.CT Cardiac Planning Recalled by Siemens Medical Solutions...
The Issue: There is a potential risk of a wrong measurement in the annulus plane during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.