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 24601–24620 of 28,488 recalls
Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...
The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box)...
The Issue: The sterile barrier in the packaging may be compromised due to cracks in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...
The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...
The Issue: A stock check revealed broken glass fibers between the connector and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...
The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Luminos dRFsystem The Axiom Luminos dRF is intended to Recalled by...
The Issue: It was determined that under rare environmental conditions (i.e., extremely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation Systems (enGen) with TCAutomation -- For in...
The Issue: Software anomaly: potential for delay in the reporting of patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems VitD 100 test Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS Recalled by Siemens...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems VitD Total 100 test Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Potential for biased...
The Issue: Potential for biased results when a Multiple Window (MW) code is associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems TSH3 Ultra Recalled by Siemens Healthcare Diagnostics,...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential for biased results when a Multiple Window (MW) code is associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.