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. 2,641 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,641 in last 12 months

Showing 92219240 of 28,488 recalls

Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Bag Access Device Recalled by CAREFUSION Due to Needle-free...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite 'Y' Extension Set 2 Needle-Free Valves Recalled by CAREFUSION...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED Recalled...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Recalled by CAREFUSION Due to Needle-free connector valves,...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity Burette Set 60 DP 3 SmartSite VALVES BALL VALVE DRIP CHAMBER...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Bag Access Device Needle-Free Valve Recalled by CAREFUSION Due...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Alaris Pump Infusion Buerette Set Smallbore Tubing Smartsite Port...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Extension Set SMALLBORE Tubing SmartSite VALVE Recalled by CAREFUSION Due...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD ADD-ON Burette Set V/NV Needle-Free Valve Recalled by CAREFUSION Due to...

The Issue: Needle-free connector valves, either standalone or attached to extension...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· Magnolia Medical Technologies, Inc.

Recalled Item: Steripath Luer Transport Pack Recalled by Magnolia Medical Technologies,...

The Issue: Product was shipped with the incorrect Transfer Adapter Instructions For Use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Paragon 28, Inc.

Recalled Item: Phantom Nail System Recalled by Paragon 28, Inc. Due to A thin wall...

The Issue: A thin wall condition between the inner cannulation and the flutes of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Leica Microsystems, Inc.

Recalled Item: BOND Ready-To-Use Primary Antibody CDX2 (EP25) Recalled by Leica...

The Issue: Product may not perform as specified in IFU.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Getinge Dominican Republic SA

Recalled Item: Arjo Disposable Repositioning Sling Recalled by Getinge Dominican Republic...

The Issue: Sling loop straps on device pose a trip hazard.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing