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 27461–27480 of 28,488 recalls
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated Recalled by...
The Issue: Embedded iron oxide glass defect which may have the potential to break off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TORQ Sternal Closure Device. The common name is TWISTER Recalled by Kardium...
The Issue: The TORQ Sternal Closure Device, Lot 062711, is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT 16 System Product Usage: The Brilliance 16 Recalled by...
The Issue: Philips was notified that the system logout in software version 2.3.6 is now...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREVI Isola System Recalled by Biomerieux Inc Due to The instrument may not...
The Issue: The instrument may not dispense the specimen onto the pre-poured media...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors...
The Issue: Inspan Compressors may break at weld causing a loss of compression
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Spectrolyse PAI-1 Recalled by Sekisui Diagnostics Llc Due to...
The Issue: SPECTROLYSE PAI-1 activity assay producing lower than expected absorbance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves...
The Issue: Trilogy Longevity Constrained Liner devices were packaged in incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-slice CT Scanner System Recalled by Philips Medical Systems...
The Issue: On August 24, 2012 the firm recalled the MX 16-slice after discovering that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The brand name is MRidium Series 1000 MR Infusion Sets Recalled by Iradimed...
The Issue: Iradimed Corporation is recalling MRidium Series 1000 MR Infusion Sets, Type...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia...
The Issue: King Systems received a customer complaint indicating that the customer had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...
The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW Recalled by Smith &...
The Issue: Modular necks were manufactured out of specification by a vendor; the taper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Rom¿ Total Hip System Poly Liner Packaging: The insert is Recalled by...
The Issue: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: Recalled...
The Issue: When using the optional S-LIFT (also known as S-LIF) Implant Guides without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: The firm is recalling the product due to some cartridges may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...
The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.