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 25281–25300 of 28,488 recalls
Recalled Item: Vascu Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...
The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nephros Dual Stage Ultra Filter (DSU) Brochure Document 60-3003 Revisions: 0...
The Issue: Promotional materials for non-medical water filtration products were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dura Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...
The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Disposable Recalled by Integra LifeSciences Corp. d.b.a. Integra...
The Issue: Integra LifeSciences Corporation is recalling certain lots of Integra Kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 3T MRI System Recalled by Toshiba American Medical Systems Inc Due to...
The Issue: Toshiba America Medical Systems, Inc. is recalling due to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-HBs Calibrators & VITROS Anti-HBs Reagent Packs Recalled by...
The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of Recalled by Roche...
The Issue: There is a software synchronization issue with the ACCU-CHEK Combo system....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Security (TM) Enclosed Carpal Tunnel System Blade ( Recalled by Biomet, Inc....
The Issue: Security Blades were manufactured oversized and potentially won't advance or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Accolade II 127 Neck Angle Hip Stem Recalled by Stryker Howmedica...
The Issue: Stryker received a report from the field indicating that an Accolade II Hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) List number 126970465 labeled in part: 12697-65 LifeShield Recalled...
The Issue: Several lots of the LifeShield Latex-Free HEMA Y-Type Blood Set IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Civco Belly Board MRI Recalled by Civco Medical Instruments Inc Due to...
The Issue: Scales adhered to the product may be misaligned from the zero such that one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery NMCT 670 Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Civco Belly Board Recalled by Civco Medical Instruments Inc Due to Scales...
The Issue: Scales adhered to the product may be misaligned from the zero such that one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osseocare Pro Console & Set Osseocare Pro Recalled by Nobel Biocare Usa Llc...
The Issue: The recall was initiated because there is a potential for malfunction of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD...
The Issue: Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Series: Clinac Recalled by Varian Medical Systems, Inc. Due to This...
The Issue: This correction is to notify users that a solution to a previous correction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.