Oregon Recalls

4,658 recalls on record affecting Oregon

medical Class II
2017-01-04

Shimadzu Medical Systems recalls Shimadzu X-ray TV System, Catalog No. SONIALVISION G4

Shimadzu Medical Systems is recalling Shimadzu X-ray TV System SONIALVISION due to possibility of oil leaking from the x-ray tube housing under certain conditions.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls The OEC 9900 Elite mobile fluoroscopy system is designed to

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-18

Stryker Sustainability Solutions recalls Reprocessed Electrophysiology Catheter Cables Catalog Numbe

A breach in the sterile packaging may have occurred resulting in potentially non-sterile product.

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medical Class II
2017-01-18

Stryker Sustainability Solutions recalls Reprocessed Ablation Catheter Cable Catalog Number: CR3425C

A breach in the sterile packaging may have occurred resulting in potentially non-sterile product.

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medical Class II
2017-01-18

Varian Medical Systems, Inc. recalls Eclipse Treatment Planning System version 13.MR2 [13.06.31

Modifications in version 13.6MR2 for Contouring, SmartAdapt, and SmartSegmentation workspaces resulted in contours not being saved consistently in Eclipse. Treatment Planning System. The issue only occurs if certain conditions are fulfilled.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 680

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is des

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-18

C.R. Bard, Inc. recalls SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Tempe

The product contained a latex catheter instead of a silicone catheter.

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medical Class II
2017-01-25

Elekta, Inc. recalls Monaco RTP System. Used to make treatment plans for patie

Incorrect dose after editing beam number an wedge angle.

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medical Class II
2017-02-01

Acumedia Manufacturers, Inc. recalls Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50K

light precipitate may form in prepared plates of Acumedia Tryptic Soy Agar (7100) Lot# 108166. While there is no change in growth performance of this medium, the formation of particulate matter may be misinterpreted as growth in poured plates thereby leading to inaccurate counts.

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medical Class II
2017-02-08

Implant Direct Sybron Manufacturing, LLC recalls SwishTapered Implant

The extender product code (9037-03) that is packaged with the SwishTapered (Part Number 933308; Lot Number 73241) Implant was packaged in the incorrect position. This discrepancy may lead to the possibility of extender not seating properly on the implant, which may lead to micro-leakage and a possible infection to the patient.

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medical Class II
2017-02-15

Angiodynamics Inc. (Navilyst Medical Inc.) recalls Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distri

The Celerity ECG Cable Accessory Pack has the potential to contain an ECG Clip Cable that was not properly manufactured. The affected product is not soldered per specification, and may result in the device not properly conducting the ECG signal.

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medical Class II
2017-02-15

Invacare Corporation recalls Foot Section - BAR5490IVC

A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.

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medical Class II
2017-02-15

Teleflex Medical recalls Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and She

Labeling inconsistency - units labeled with a 7mm tube may contain a size 6.5mm tube, and units labeled 7.5mm tube may contain a size 5.5mm tube.

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medical Class II
2017-02-15

Invacare Corporation recalls Bariatric Bed - BAR600IVC

The junction box used in the bariatric bed may emit sparks and result in a fire.

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medical Class II
2017-02-15

Invacare Corporation recalls Junction Box - 1104343 and 1193560

A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.

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medical Class II
2017-02-15

Invacare Corporation recalls Bariatric Bed - BARPKG-IVC 1633

A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.

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medical Class II
2017-02-22

Philips Medical Systems (Cleveland) Inc recalls BrightView XCT

The intended use listed in the English and localized language IFUs for BrightView XCT systems did not match the intended use documented in the 510K submission.

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medical Class II
2017-02-22

Philips Medical Systems (Cleveland) Inc recalls BrightView X upgraded to XCT 882454

The intended use listed in the English and localized language IFUs for BrightView XCT systems did not match the intended use documented in the 510K submission.

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medical Class III
2017-03-01

Applied Medical Technology Inc recalls AMT Bridle - Nasal Tube Retaining System Used with Nasoga

Expired expiration dates are listed on the pouches.

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Showing 20 of 4,658 recalls. Use search to filter further.