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. 2,567 recalls have been distributed to Oregon in the last 12 months.
Showing 16001–16020 of 28,488 recalls
Recalled Item: RECON DRILL 6MM X 439MM Recalled by Zimmer Biomet, Inc. Due to The firm is...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XLTEK EMU40EX EEG Headbox Recalled by Natus Neurology DBA Excel Tech., Ltd....
The Issue: Possible degradation of an internal electronic component over time which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAREstream ProNox Nitrous Oxide Delivery System labeled as the following:...
The Issue: Two analgesic gas delivery system oxygen/nitrous oxide mixers were reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MegaPower Electrosurgical Generator Recalled by Megadyne Medical Products,...
The Issue: If two devices are plugged into the same channel/port in the generator, both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...
The Issue: In vitro diagnostic devices, used greater than 6 months after date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...
The Issue: Possible diminished performance prior to its established expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...
The Issue: Blades are loose in handles and may fall out due to non cured epoxy
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. This corrective action...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...
The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...
The Issue: Out of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Distributed by Medtronic Recalled by FHC, Inc....
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Lead Adapter for STar" Drive Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Manual) Distributed by Medtronic...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.