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Oregon Scientific Inc., of Tualatin, Ore.

Oregon Scientific Inc., of Tualatin, Ore. Recalls

All product recalls associated with Oregon Scientific Inc., of Tualatin, Ore..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 33641–33660 of 37665 recalls

Weather Radios (Oregon Scientific) – Alert Failure (2007)

This recall involves the following Weather Radios and Weather Stations: NAME MODEL All Hazards Portable Weather Alert Radio WR103NX Portable Public Alert Radio WR108 Public Alert Weather Station WRB308 John Deere Public Alert Weather Station WRB308J No other models are included in this recall.

CPSCAug 29, 2007Nationwide• Oregon Scientific Inc., of Tualatin, Ore.

Boston Scientific Corporation: Boston Scientific Radial Jaw Large Capacity Biopsy Forcep...

Device lacked manufacturing finishing process resulting in endoscope damage.

FDAAug 28, 2007Nationwide• Boston Scientific Corporation

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 7...

An issue with the Paceart System - 2006 First Edition (Get Connected Edition) exists. Under certain circumstances, Paceart System Generic ICD reports may not accurately reflect patient VT/VF, SVT/NST and Mode Switch/AT/AF episode detection data. When episode detection data is imported into the Paceart System from certain sources, the Paceart System Generic ICD reports display a zero, suggesting

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FDAAug 27, 2007Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Sofamor Danek USA Inc: Medtronic Sofamor Danek, TSRH SiLo 5.5 Spinal System, Sag...

Disassembly: The movable cradle component could detach from the saddle under extreme manipulation of the associated rods prior to final tightening of the set screws.

FDAAug 24, 2007Nationwide• Medtronic Sofamor Danek USA Inc

BatteryZone, Inc.: life+cel, Replacement Battery for Cardiac Science Powerhe...

Marketed without 510 (K) approval

FDAAug 24, 2007Nationwide• BatteryZone, Inc.

Philips Medical Systems North America Co. Phillips: Philips Medical System - BV Pulsera Mobile C-arms with Re...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Medical System - Endura X-Ray Systems (Release 2)...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Sleepi Crib Mattresses (Stokke) – Entrapment Risk (2007)

Only oval shaped Sleepi cribs with foam mattresses sold under the following model numbers are the subject of this recall: 660321, 660320, 660301,660305, 660318, 652268, 652269, 652246, 652247 and 652248. The cribs were sold in a variety of colors, including white, walnut, natural, cherry and whitewash. The model number can be found on the packaging and underside of the crib.

CPSCAug 23, 2007Nationwide• Stokke, of Kennesaw, Ga.

Trucks Shaker Teether Books (Priddy) – Choking Hazard (2007)

Choking Hazard

The recalled cloth teether book, entitled "trucks", has a yellow dump truck on the front cover on a blue background. Attached to the top of the book is a yellow rattle with a green teether attached on the right side of the rattle and an orange teether attached to the left side of the rattle.

CPSCAug 23, 2007Nationwide• St. Martin's Press, LLC, of New York, N.Y.

Ambu Incorporated: Ambu, Positive End Expiratory Pressure (PEEP) Valves, PEE...

Lower pressure than expected: Medical device for respiratory care may leak and not register accurate flow settings that affect patient respiration.

FDAAug 21, 2007Nationwide• Ambu Incorporated

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew, CALAXO Bioabsorbable lnterference Screw, ...

Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation.

FDAAug 21, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Inotech Biosystems Intl., Inc: Inotech brand Heparin Adsorbant, Catalog #: HA-1, in 10m...

Erroneous Coagulation Tests

FDAAug 20, 2007Nationwide• Inotech Biosystems Intl., Inc

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with Data Innovatio...

Labeling provided by two integrated software systems are not clear enough to avoid potential demographic and sample type mismatches under certain conditions.

FDAAug 20, 2007Nationwide• Beckman Coulter Inc

Stryker Howmedica Osteonics Corp.: Howmedica Osteonics Corp., Scorpio NRG Femoral Size 7 Rig...

A box labeled as a Scorpio NRG Femoral Size 7 Right, may actually contain a Scorpio PS Femoral Size 5 Right.

FDAAug 20, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Equipment, Fluid Management Stand, for Fluid Manage...

Outflow Difference: The accuracy of the Equimat displayed value could be influenced by external factors of the cart/stand and may result in a fluctuating or inaccurate reading.

FDAAug 17, 2007Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe

N.I.C.E. Navigation System (Kiryung) – Fire Hazard (2007)

Fire/Burn Risk

The N.I.C.E. P200 is a black portable navigation and entertainment device that can be attached to a vehicle's windshield. The device has a 4-inch touch screen LCD monitor and contains one lithium battery. "Clarion" and "N.I.C.E. P200" are printed on the device. "Clarion NAVBATTERY" is printed on the battery. The recall includes any N.I.C.E. P200 in which batteries were previously replaced.

CPSCAug 16, 2007Nationwide• Kiryung Electronics of Seoul, South Korea

Alphatec Spine, Inc.: Novel PEEK VBR XS 16-22 MM, S-5, 20MM, Part Number: 64733...

Firm confirmed that two lots were mixed during manufacturing and were incorrectly labeled with the wrong part number & lot number. They were incorrectly laser marked with the wrong part numbers and sizes. Two lots were mixed from the following lot numbers: Part Number 64733-120 Lot Number 611884, and Part Number 64753-126 and Lot Number 611881.

FDAAug 16, 2007Nationwide• Alphatec Spine, Inc.

Skil Circular Saws (Bosch) – Laceration Hazard (2007)

Laceration Risk

The recall involves Skil® brand circular saws with model numbers 5650, 5700, 5750 and 5755. The model number and date code are printed on the nameplate located on the front of the saw. The recall includes the following date codes: 28101 - 29231 38101 - 39231 48101 - 49231 58101 - 59231 68101 - 69231 No other models or date codes are included in this recall.

CPSCAug 15, 2007Nationwide• Robert Bosch Tool Corp., of Mount Prospect, Ill.

The Braun Corporation: Braun wheelchair lift, model NL, Braun Corporation, Wina...

The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.

FDAAug 15, 2007Nationwide• The Braun Corporation

Baxter Healthcare Corp. Rt.: Baxter Colleague CX Single Channel Volumetric Infusion Pu...

Some of the pumps were upgraded by one service technician who failed to replace prisms and batteries as required in the upgrade.

FDAAug 15, 2007CA, FL• Baxter Healthcare Corp. Rt.