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. 2,432 recalls have been distributed to Oregon in the last 12 months.
Showing 37901–37920 of 50,914 recalls
Recalled Item: TESTOSTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITAMIN B-COMPLEX Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METHYLCOBALAMIN PRESERVATIVE FREE PREFILLED Recalled by JD & SN Inc., dba...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DMPS (DIMERCAPTO-PROPANESULFONIC NA (SINGLE USE ONLY) Recalled by JD & SN...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLUTATHIONE MDV Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHORIONIC GONADOTROPIN Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METHYLCOBALAMIN MDV Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADRUCIL (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Presence of Particulate Matter: silcone rubber and fluorouracil crystals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: univasc (moexipril HCl) tablets Recalled by Ucb, Inc Due to Failed...
The Issue: Failed Dissolution Testing: Failed 24 month dissolution testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due...
The Issue: EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC) Recalled by...
The Issue: customers are receiving a high number of Abnormal Assay Errors or are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips GoSafe Mobile Help Button Recalled by Lifeline Systems, Incorporated...
The Issue: Irregular battery disconnection resulted in issues with Mobile Health Button...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER LH Series Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument for Sternal ZIPFIX Recalled by Synthes (USA)...
The Issue: The end cap may loosen and detach making the instrument non-functional. No...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Pioneer Plus Re-Entry Catheter Recalled by Volcano Corporation Due...
The Issue: Due to a manufacturing defect, there is the possibility that a small wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft...
The Issue: Biomet has initiated a recall on Biomet Spine Lineum OCC Starter Flexible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER ISOTON 4 Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to Channel Error...
The Issue: Channel Error code is displayed on the PC unit with an audio and visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.