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Showing 89541–89560 of 92409 results

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Misys Healthcare Systems: Misys Laboratory System, versions 5.3 build 63 through 5....

Incorrect demographics display which can result in incorrect information being used in diagnosis or treatment of patients.

FDAJul 21, 2003Nationwide• Misys Healthcare Systems

Roche Diagnostics Corp.: Disetronic H-TRON V100 Insulin Pump; catalog # 8010030C [...

Lack of assurance of reliability, due to quality system regulations violations, plus notice to users not to expose pump to water.

FDAJul 21, 2003Nationwide• Roche Diagnostics Corp.

Alcon Laboratories, Inc.: ''Alcon Ladarwave CustomCornea Wavefront System'' Aberrom...

Software error could, under specific circumstances, allow the patient's centration images and data to be stored incorrectly.

FDAJul 21, 2003Nationwide• Alcon Laboratories, Inc.

Perkinelmer Life Sciences, Inc.: Anti-dsDNA [125I] Radiobinding Assay Kit. For In-Vitro Di...

Product's outer carton label was labeled with an extended expiration date

FDAJul 21, 2003CA, IN, MO +1 more• Perkinelmer Life Sciences, Inc.

Roche Diagnostics Corp.: Disetronic H-TRONplus Insulin Pump; catalog # 8050023 [cl...

Lack of assurance of reliability, due to quality system regulations violations, plus notice to users not to expose pump to water.

FDAJul 21, 2003Nationwide• Roche Diagnostics Corp.

Varian, Inc.: On-Site Alcohol IVD A single use enzymatic assay for qua...

Stability in question.

FDAJul 18, 2003Nationwide• Varian, Inc.

Philips Medical Systems Sales & Service Region No. America: Diagnost 97

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: OmniDiagnost System

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Stryker Howmedica Osteonics: Femoral Resection Guide, Scorpio L.R.S. Instrumentation.

Scorpio Femoral Resection Guides have the potential to remove more bone than necessary.

FDAJul 17, 2003IN• Stryker Howmedica Osteonics

Oil Lamp Boxed Sets (DesignPac) – Flammability Risk (2003)

The boxed sets contain a clear vase with pink or purple floral designs, and a 16-ounce bottle of paraffin oil. The packaging is labeled "Handpainted Oil Lamp Set" and "Floral Garden." Item number 054 11 0229 is printed on the packaging.

CPSCJul 17, 2003Nationwide• DesignPac, of Northlake, Ill.

Novelty Cigarette Lighters (De Bon Sales) – Design Hazard (2003)

There are two styles of lighters included in this recall. The first is a chrome and silver lighter, in the shape of a rearing horse. It is about 2.3 inches long and is labeled "DE-L-36." The second lighter is silver-colored, in the shape of a bird head holding a snake. It is about 2.5 inches long and is labeled "DE-L-23."

CPSCJul 17, 2003Nationwide• De Bon Sales Inc., of Houston, Texas

Slow Cookers (Hamilton Beach) – Electrical Safety Risk (2003)

The recalled slow cookers were sold under the Hamilton Beach and Proctor-Silex brand names, which are printed on the front of the base of the unit. The slow cookers are either round or oval, and were sold in solid white and various print designs. They have a capacity of 3.5 to 6.5 quarts. The slow cookers have series codes A through D which are printed on the bottom along with the model number. Brand Names Model Numbers Hamilton Beach 33390, 33475, 33575, 33590, 33675, 33690, 33725, 33850, 33860 Hamilton Beach / Portfolio 33680 Proctor-Silex 33320, 33320FD, 33325, 33375, 33380, 33625A

CPSCJul 17, 2003Nationwide• Hamilton Beach/Proctor-Silex, of Glen Allen, Va.

Smart Dive Computers (UWATEC) – Potential Malfunction (2003)

The recalled units are the UWATEC Smart PRO and the Smart COM dive computers. The Smart PRO is offered as a console and as a wrist unit. The Smart COM only comes in a console model. The names of each unit appear on the computer case, along with the name "UWATEC."

CPSCJul 17, 2003Nationwide• UWATEC AG, of Hallwil, Switzerland

Toad Lawn Ball Sprinkler (Midwest) – Design Defect (2003)

The green, frog-shaped sprinkler is 6-1/2 inches long, 6-1/2 inches wide and 7 inches tall. The recalled lawn balls have a label on the bottom that includes the model number 738449 508893 and the words, "Made in China."

CPSCJul 17, 2003Nationwide• Midwest, of Cannon Falls, Minn.

Baxter Healthcare Corp. Rt: Vented Solution Set, 10 drops/mL, 92'', Luer Activated Va...

There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.

FDAJul 16, 2003Nationwide• Baxter Healthcare Corp. Rt

Baxter Healthcare Corp. Rt: Interlink System Solution Set with Microbore Tubing, 60 D...

There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.

FDAJul 16, 2003Nationwide• Baxter Healthcare Corp. Rt

Baxter Healthcare Corp. Rt: Fenwal Blood Component Recipient Set with Standard Blood ...

There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.

FDAJul 16, 2003Nationwide• Baxter Healthcare Corp. Rt

Baxter Healthcare Corp. Rt: Baxter Vented Nitroglycerin Set, 105'', PVC Tubing Segmen...

There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.

FDAJul 16, 2003Nationwide• Baxter Healthcare Corp. Rt

Baxter Healthcare Corp. Rt: Fenwal Straight Type Blood Set with Large Standard Blood ...

There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.

FDAJul 16, 2003Nationwide• Baxter Healthcare Corp. Rt

Unknown Manufacturer: Boston Scientific Scimed Monorail Express 2 Coronary Sten...

There is an Increased potential for broken struts of the stents.

FDAJul 16, 2003Nationwide

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