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. 2,486 recalls have been distributed to Oregon in the last 12 months.
Showing 22641–22660 of 28,488 recalls
Recalled Item: 4.0mm Variable Angle Recalled by Alphatec Spine, Inc. Due to Mislabeling
The Issue: During a field audit it was discovered by an employee that a 16mm Trestle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...
The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...
The Issue: Some rods may not meet the appropriate traceability requirements including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...
The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...
The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...
The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation...
The Issue: Baxter Corporation is conducting a field action for the ABACUS SE and ME...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assay Data Disk (ADD) Recalled by Ortho-Clinical Diagnostics Due to Software...
The Issue: Software anomaly regarding urine samples that require acidified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly allows testing of multiple assays using a single urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly allows testing of multiple assays using a single urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Logicon Caries Detector Product Usage: Analyze inter-proximal tooth surfaces...
The Issue: GA Industries is recalling the Logicon Caries Detector, version 5.0, for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly...
The Issue: Software anomaly regarding urine samples that require acidified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion AVEA ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: A pressure transducer failure can develop, activating a false Extended High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for...
The Issue: In some Flow-i Anesthesia Systems, patient cassette can get dislodged which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Care Cliner X-Large - with Nylon Casters Oncology Recalled by Winco...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Drop Arm Care Cliner Standard - with Steel Casters Oncology Recalled...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Inverness 24-Hour Treatment Recliner - with Nylon Casters Lay Recalled...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Nocturnal Elite Care Cliner - with Nylon Casters Lay Recalled by Winco...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Drop Arm Care Cliner X-Large - with Nylon Casters Oncology Recalled by...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.