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. 2,499 recalls have been distributed to Oregon in the last 12 months.
Showing 21461–21480 of 28,488 recalls
Recalled Item: CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...
The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost stationary X-ray system Recalled by Philips...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension EXL with LM STM Product Recalled...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Bone Awl Recalled by Aesculap, Inc. Due to The flexible shaft of...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Screw Driver SJ706R Recalled by Aesculap, Inc. Due to The flexible...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tray Set containing multiple instruments and may contain the flexible bone...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Drill Recalled by Aesculap, Inc. Due to The flexible shaft of the...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost stationary X-ray system Recalled by...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.