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. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 26901–26920 of 28,488 recalls
Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Recalled by ConMed Corporation Due to ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade Recalled...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUR/Endoscopic Cable Recalled by ConMed Corporation Due to ConMed received...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED(R) ELECTROSURGICAL SAFETY HOLSTER Recalled by ConMed Corporation Due...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle...
The Issue: BacT/ALERT SA Culture Bottle lot 1031866 may contain bottles with uncured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD¿ Composite Series Base Unit Standard Recalled by Integra...
The Issue: Integra determined there is a possibility that the Base Units may break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...
The Issue: Limited number of individual contact lens packages may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1-DAY ACUVUE MOIST Brand Contact Lenses Recalled by Johnson & Johnson Vision...
The Issue: Limited number of individual contact lens packages may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicBrainEX Product Usage: nordicBrainEx is an image processing software...
The Issue: There is an error related to the relative geometry between fiber tracts in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog...
The Issue: Reports of handle fracture and subsequent disassociation of cam assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Philips Healthcare received reports from the field stating the patient table...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Recalled by...
The Issue: A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1" instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Recalled by...
The Issue: Single needle packs in each case ( 10 needles per case) are mislabeled on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO Sensar Intraocular Lenses (IOLs) Recalled by Abbott Medical Optics Inc...
The Issue: Two production orders of these IOLs that contain mislabeled IOLs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer...
The Issue: CareFusion is recalling the SmartSite¿ Gravity Blood Set as a result of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HealthTronics Endocare 3.8mm RenalCryo Cryoprobe Recalled by Healthtronics,...
The Issue: The Endocare 3.8mm RenalCryo Cryoprobe is being recalled because the label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate Balloon Guide Catheter Recalled by Concentric Medical Inc Due to...
The Issue: Firm received complaints of resistance and possible collapse of the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.