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 27541–27560 of 28,488 recalls
Recalled Item: Invacare¿ I-Fit" Shower Chair (Models 9780 Recalled by Invacare Corporation...
The Issue: On August 6, 2012, Invacare voluntarily recalled the Invacare¿ I-Fit" Shower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....
The Issue: During the manufacturing of the affected lot a manufacturing error has led...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precise Digital Accelerator Delivery of radiation to defined target volumes...
The Issue: There have been a small number of instances in hospitals where the joint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic...
The Issue: There is a possibility that the ISKD limb lengthener may stop distracting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...
The Issue: The seat could break as a result of damage resulting from a seat belt being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP CTS PN 0000280020 ACL TOP is a bench top...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 and HT70 Plus Ventilators Recalled by Newport Medical...
The Issue: May emit a continuous high priority alarm and the ventilator may stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The patient support may move in an unintended manner if the foot switch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 PN 0000280010 ACL TOP is a bench top...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an...
The Issue: Cartridges are leaking. The leaking is observed when opening the wrapper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP (Base) PN 0000280000 ACL TOP is Recalled...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien)...
The Issue: Potential failure of HALO Energy Generator to enter "stand by" mode when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medstream 81" (206 cm) 20 Drop Standard bore Universal Administration...
The Issue: Devices leaking at the Y-site
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Brivo XR385 DR-F/ X-Ray System X-Ray System Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The...
The Issue: Ethicon Endo-Surgery initiated this voluntary global recall for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osseotite Tapered Certain Implant 5 X 10mm Model INT510 Biomet Recalled by...
The Issue: Biomet 3i recalled their Osseotite Tapered Certain Implant, Model # INT510...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 CTS PN 0000280050 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.