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 19741–19760 of 28,488 recalls
Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...
The Issue: If an affected Patient Monitor has been powered on continuously for several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled...
The Issue: Terumo Custom Cardiovascular Procedure Kits are labeled as Xcoating surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRI Salicylate Serum Tox Assay Recalled by Microgenics Corporation Due to...
The Issue: Some lots of DRI Salicylate Serum Tox Assay negative patient samples are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to A firmware...
The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Recalled by GE OEC Medical Systems, Inc Due to A firmware issue in...
The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large QWIX Compression screw Recalled by Integra LifeSciences Corp. Due to...
The Issue: Labeling on the Qwix Screw product states that it is a "compression screw"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen Recalled by...
The Issue: Device can fail during operation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS Sterile Transparent Film and all the RENASYS Dressing kits Recalled...
The Issue: Sterility seal integrity failures on the Renasys Sterile Transparent Film
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Recalled by...
The Issue: Incorrect drill protocol in the Instructions for Use (IFU)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology CT Model number 728244 Product Usage: Computed...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE IMPERVIOUS GOWN WITH THUMBHOOKS Recalled by Cardinal Health Due to Blue...
The Issue: Blue Impervious Gown with thumbhooks, X-large. All lots do not meet design...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain 3.0.0 Usage: The device is intended for the Recalled by Zimmer...
The Issue: Communication errors between ROSANNA BRAIN software, MARIO software and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.