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. 2,567 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,567 in last 12 months

Showing 1650116520 of 50,914 recalls

Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Bulk Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Sterile Recalled by Cardinal Health 200, LLC Due...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Bulk Non-Sterile Recalled by Cardinal Health 200, LLC...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Potential of products...

The Issue: Potential of products packaged for lot 323-108-7 were packaged in pouches...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 24, 2021· Arthrex, Inc.

Recalled Item: Drill Bit Recalled by Arthrex, Inc. Due to The color indicator on the...

The Issue: The color indicator on the proximal end of the shaft of the AR-8770-02 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Philips CT systems are advanced continuous-rotation computed tomography...

The Issue: Philips has internally detected an issue with the actuators used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2021· Trinity Sterile, Inc.

Recalled Item: Midline Catheter Dressing Change Kit with Statlock - Product Usage: Recalled...

The Issue: Evidence of face masks or other material in the seal in several kits,...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...

The Issue: Subpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 22, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to For some LINAC...

The Issue: For some LINAC types, merging clinical beams with beams of approximate dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI Recalled by...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Sirtex Medical Limited

Recalled Item: SIROS D-Vial Prep Set Recalled by Sirtex Medical Limited Due to There is a...

The Issue: There is a potential presence of particulate matter in the D-Vial.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...

The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...

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

Class II — Potential Health HazardOngoing
DrugFebruary 19, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Methylprednisolone Tablets USP Recalled by Jubilant Cadista Pharmaceuticals,...

The Issue: Labeling: Illegible label: Customer complaint received of mis-alignment...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund