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.

50,914 total recalls
2,470 in last 12 months

Showing 2502125040 of 28,488 recalls

Medical DeviceDecember 10, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator with CO2/EtCO2 Measurement The...

The Issue: MRx defibrillator displays a -?- for EtCO2 and does not display EtCO2 values...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Zimmer, Inc.

Recalled Item: Versys Build-Up Block The VerSys CRC Hip System is indicated Recalled by...

The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Chow Illuminated Pick (Dull) Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Wide Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Standard tubing set Recalled by Synergetics Inc Due to Faulty seals on the...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 27ga ONE-STEP (tm) Awh/Tano Vivid Chandelier Recalled by Synergetics Inc Due...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Wide Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX- Top Unit instrument Recalled by Becton Dickinson & Co. Due to...

The Issue: Improperly functioning component of a diagnostic medical device may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 25ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Gambro Renal Products, Incorporated

Recalled Item: Gambro Cartridge Blood Set Recalled by Gambro Renal Products, Incorporated...

The Issue: Occluded heparin tubing events preventing anticoagulation dosing on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· ArthroCare Medical Corporation

Recalled Item: Arthrocare SPORTS MEDICINE Recalled by ArthroCare Medical Corporation Due to...

The Issue: A sharp edge on the cannulated tip of the device may damage or cut a suture.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX 40 instrument Recalled by Becton Dickinson & Co. Due to...

The Issue: Improperly functioning component of a diagnostic medical device may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Chow Illuminated Pick Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals on the...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Mid-Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Chandelier Infusion Cannula Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Wide Field Endo Illuminator Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 27ga ONE-STEP (tm) Endo Illuminator Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing