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.

50,914 total recalls
2,457 in last 12 months

Showing 2694126960 of 28,488 recalls

Medical DeviceDecember 17, 2012· Medacta Usa Inc

Recalled Item: Medacta Quadra Trial Broach size 0 part # 01.10.10.045 Recalled by Medacta...

The Issue: The tip of the Quadra Trial Broach size 0, broke during a surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2012· Animas Corporation

Recalled Item: Animas(R) 2020 Recalled by Animas Corporation Due to Due to an internal...

The Issue: Due to an internal calendar date limit (December 31, 2015) these pumps will...

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

Class III — Low RiskOngoing
Medical DeviceDecember 17, 2012· Mizuho OSI

Recalled Item: Mizuho Orthopedic Table Recalled by Mizuho OSI Due to Possible instability...

The Issue: Possible instability of Orthopedic Table Top. If the epoxy bond fails, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2012· Intel-GE Care Innovations LLC

Recalled Item: QuietCare-Networked product Recalled by Intel-GE Care Innovations LLC Due to...

The Issue: Care Innovations detected a software anomaly: During the engineering...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Philips Healthcare Inc.

Recalled Item: Juno DRF Recalled by Philips Healthcare Inc. Due to Values of fluoroscopy...

The Issue: Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Medical Components, Inc dba MedComp

Recalled Item: Recalled by Medical Components, Inc dba MedComp Due to The affected product...

The Issue: The affected product was packaged with the incorrect introducer needle. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Ortho-Clinical Diagnostics

Recalled Item: Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption...

The Issue: Some VITROS¿ Chemistry Products Vapor Adsorption Cartridge CAT No. 6800100...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Sr Instruments Inc

Recalled Item: SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare...

The Issue: SR Instruments Inc. is implementing a field correction for the Joerns...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2012· Abbott Laboratories

Recalled Item: Abbott Laboratories Recalled by Abbott Laboratories Due to The Architect...

The Issue: The Architect 25-OH Vitamin D assay has the potential to generate falsely...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2012· Becton Dickinson & Co.

Recalled Item: BD MAX PCR Cartridges Catalog #437519 Recalled by Becton Dickinson & Co. Due...

The Issue: Cartridges are not sealing properly during PCR testing and may cause false...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2012· Toshiba American Medical Systems Inc

Recalled Item: Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device...

The Issue: Toshiba Medical Systems has received reports of startup issues with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Flowtron Trio DVT Pump Recalled by Arjo, Inc. dba ArjoHuntleigh Due to The...

The Issue: The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...

The Issue: Firm has confirmed higher imprecision with the recalled lots on Beckman...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2012· Becton Dickinson & Co.

Recalled Item: BBL(TM) Fildes Enrichment Recalled by Becton Dickinson & Co. Due to...

The Issue: Enrichment media intended to enhance the cultivation of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2012· Hill-Rom, Inc.

Recalled Item: Liko Standard Slingbar 450. The Standard Slingbar 450 is a Recalled by...

The Issue: Liko/Hill-Rom has received reports from facilities which indicate that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Emit(R) tox(TM) Serum Calibrators Recalled by Siemens Healthcare...

The Issue: Incorrect expiration date was assigned to the D1 lot of Emit(R) tox(TM)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 5, 2012· SynCardia Systems Inc.

Recalled Item: Companion External Battery Recalled by SynCardia Systems Inc. Due to...

The Issue: Syncardia Systems is recalling the Companion External Batteries used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2012· Canon Inc.

Recalled Item: Canon Full Auto RK-F2 Recalled by Canon Inc. Due to Canon Inc. had received...

The Issue: Canon Inc. had received 17 claims from our foreign sales companies between...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: B. Braun Medical Inc. is informing our customers of a field correction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2012· Abbott Molecular

Recalled Item: Abbott m2000sp Instrument Recalled by Abbott Molecular Due to An issue with...

The Issue: An issue with the m2000sp Instrument software has been identified whereby,...

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

Class II — Potential Health HazardOngoing