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. 2,470 recalls have been distributed to Oregon in the last 12 months.
Showing 24141–24160 of 28,488 recalls
Recalled Item: Sarns Malleable Venous Return Cannulae 24 Recalled by Terumo Cardiovascular...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB Catheter Kit Product Usage: Venous Return Cannula is indicated Recalled...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns D4 Aortic Arch Cannulae 6.0mm Recalled by Terumo Cardiovascular...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Reduced Neck Standard & Extended Offset Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Potential loss of airway...
The Issue: Potential loss of airway gas measurement in the Compact Airway Gas Modules....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Although the Natural Rubber Latex...
The Issue: Although the Natural Rubber Latex caution symbol is clearly displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500...
The Issue: RAPIDPoint 500 Measurement Cartridges may have an error code one or more...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.0mm Barrel Bur Sterile Recalled by Stryker Instruments Div. of...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 6.0mm Egg Bur Sterile Product Usage: The devices are Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lindemann Drill Short Recalled by Stryker Instruments Div. of Stryker...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDComm¿ Data Management System. The RAPIDComm¿ Data Management...
The Issue: RAPIDComm¿ 5.0 Screen Layout will display incorrect test names
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 4.0mm Round Fluted Bur Sterile Product Usage: The devices Recalled...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 3.0mm Round Fluted Bur Aggressive Sterile Product Usage: The...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 3.0mm x 3.8mm Neuro Drill Sterile Product Usage: The Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1.5mm Wire Pass Drill Sterile Product Usage: The devices Recalled by...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 5.0mm Round Fluted Bur Aggressive Sterile Product Usage: The...
The Issue: There may be missing notches, partial notches or no notches at all in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.