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Clark Research and Development Inc Number

Clark Research and Development Inc Number Recalls

All product recalls associated with Clark Research and Development Inc Number.

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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 34121–34140 of 37665 recalls

Clark Research and Development Inc Number: Clark Biocompatible Hemoperfusion Cartridge, Sorbent: He...

Lack of sterility assurance based on lack of sterility validation for labeled sterilization directions

FDAJan 19, 2007Nationwide• Clark Research and Development Inc Number

Smith & Nephew, Inc. Endoscopy Division: RF Denervation Probe, 10 cm, temperature sensing electrod...

Product is non-sterile but labeled incorrectly as sterile.

FDAJan 19, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Smiths Medical MD, Inc.: Deltec branded CADD-Prizm PCS II ambulatory infusion pump...

The year of manufacture had been incorrectly entered as 1980 into the pumps software during the manufacture process. As a result the pump may go into an immediate 'Clock battery is Low/Service Immediately' or 'Clock Battery needs service soon' alarm message indicating that the pump requires servicing.

1...1705 170617071708 1709...1884

Page 1707 of 1884Next

FDAJan 19, 2007Nationwide• Smiths Medical MD, Inc.

Smith & Nephew, Inc. Endoscopy Division: RF Denervation Probe, 15 cm, temperature sensing electrod...

Product is non-sterile but labeled incorrectly as sterile.

FDAJan 19, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Graco Contempo Highchairs – Collapse Risk (2007)

The Contempo™ highchairs have an "A" frame design. The highchairs feature six height adjustment positions and three recline positions. The recalled highchairs have model numbers that begin with 3800, 3803, 3804, 3805, 3810 and 3811 followed by a three-letter fashion code. Model numbers included in the recall include: 3800COU, 3800DRB, 3800FMT, 3800GGG, 3800GRM, 3800HEM, 3800JEN, 3800LEG, 3800MNS, 3800OWD, 3800SND, 3800TFE, 3800RIT, 3803HRL, 3804CNR, 3805BDA, 3810PEW, 3810PST and 3811PST. The highchairs were manufactured from October 27, 2005 through November 22, 2006. The model number and manufacturing date are printed underneath the snack tray of these highchairs.

CPSCJan 18, 2007Nationwide• Graco Children's Products Inc., of Exton, Pa.

Target Baby Rattles – Choking Hazard (2007)

Choking Hazard

This recall involves plush rattles and frame ornaments sold in the "See. Spot. Save." department of Target stores. The two styles of rattles include a pink bear and a green moose. The plush animals either have a rattle inside or a plastic ring attached. The photo frame ornaments are a pink bear or green moose holding either a square or heart-shaped frame.

CPSCJan 18, 2007Nationwide• Target, of Minneapolis, Minn.

Catch Incorporated: Homocysteine Reagent Test Kit. The Homocysteine test ki...

A high homocysteine level can be reported as falsely low.

FDAJan 18, 2007CA, PA• Catch Incorporated

Radiometer America Inc: ABL800 FLEX Series analyzer with FLEXQ module-equipped w...

In some situations pre-registered patient data is not reset when leaving the pre-registration mode in the software. This occurs when a Safe Pico blood sampler associated with a specific patient is pre-registered in the analyzer by scanning a barcode.

FDAJan 16, 2007AL, CA, CO +12 more• Radiometer America Inc

GE OEC Medical Systems, Inc: OEC Uroview 2800 fluoroscopic x-ray system with 3 Phase P...

Uroview 2800 system with 3 Phase Power Distribution Box (Wonder Box) option can present a shock hazard to the user if the access door to the power box is not completely closed when the unit is powered on. .

FDAJan 15, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC Uroview 2800 with Dual Monitor Option, fluoroscopic x...

Uroview 2800 system with dual monitors may pose a safety risk to patients if the monitors become disconnected and fall.

FDAJan 15, 2007Nationwide• GE OEC Medical Systems, Inc

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation; for diagnostic ima...

The Centricity PACS RA1000 Workstation Software may manifest certain mammography image display problems only if the images were acquired through GE Senographe versions 2000D, DS or Essential.

FDAJan 12, 2007Nationwide• GE Healthcare Integrated IT Solutions

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 80...

The hand crank may crack in the bearing/shaft area due to a manufacturing defect. (Note: Some of the hand cranks subject to this recall were shipped as replacements for hand cranks recalled in the Summer of 2006.)

FDAJan 12, 2007Nationwide• Terumo Cardiovascular Systems Corp

Philips Medical Systems (Cleveland) Inc: No packaging. The device is a computed tomography scanne...

When the Extended Display Firled ov View reconstruction is used, the CT numbers and anatomy in teh extended region are not accurate.

FDAJan 9, 2007AR, CA, FL +16 more• Philips Medical Systems (Cleveland) Inc

Cannondale Road Bicycles – Brake Failure (2007)

The recalled road racing bicycles are made from aluminum and carbon fiber or all carbon fiber. The model name is printed on the bicycle's top tube. They were sold in the following colors: natural aluminum/carbon, red, black or black and blue. Recalled models include: Cannondale Models 2007 Six 13 Team 1 2007 Six 13 Team 1/Compact Drive 2007 Synapse Carbon SL1/Compact Drive Si Crank 2007 Synapse Carbon SL1/Standard bottom bracket, Dura Ace Crank

CPSCJan 9, 2007Nationwide• Cannondale Bicycle Corp., of Bethel, Conn.

Philips Medical Systems (Cleveland) Inc: No packaging. The device is a computed tomography scanne...

When the Extended Display Firled ov View reconstruction is used, the CT numbers and anatomy in teh extended region are not accurate.

Class IIModerate

FDAJan 9, 2007AR, CA, FL +16 more• Philips Medical Systems (Cleveland) Inc

Skytron, Div. The KMW Group, Inc: Skytron Infinity Series surgical light, 4 bulbs in 1 - 22...

If the mounting plug is improperly adjusted, the unit could separate, come apart, and fall from the mount.

FDAJan 8, 2007Nationwide• Skytron, Div. The KMW Group, Inc

Skytron, Div. The KMW Group, Inc: Skytron Infinity series (also called Astro series) minor ...

If the mounting plug is improperly adjusted, the unit could separate, come apart, and fall from the mount.

FDAJan 8, 2007Nationwide• Skytron, Div. The KMW Group, Inc

Children's Overalls (Samara Brothers) – Lead Snaps (2007)

This recall involves two styles of children's overall sets. One set is a red plaid denim overall with a white shirt trimmed in red, sold in sizes 12 through 24 months. The other set is a navy blue corduroy overall with a white shirt trimmed in green, sold in sizes 3 through 9 months. Both styles have decorative train appliqués on the front of the overalls. The collar tag of the overalls reads, "Starting Out."

CPSCJan 5, 2007Nationwide• Samara Brothers LLC, of New York, N.Y.

Gas Pool Heaters (Pentair) – Carbon Monoxide Danger (2007)

The recall involves Pentair MiniMax® NT STD Gas Pool Heaters installed indoors. They have BTU ratings between 200,000 and 400,000, and use either natural gas or propane. The model number is located on the rating plate on the inner front panel of the heater. The following model numbers are included: 460427 through 460430 460439 through 460450 460531 through 460538 460543 through 460566 The heater identification number is located on the rating plate on the inner panel of the heater, which will show "NT" and "STD" in the third and fourth blocks of the number. The recall includes units with serial numbers 0606002 and lower. The recall also includes units without serial numbers. If the unit has a serial number, it is written on the data plate on the heater, which is located on the inner front door of the heater. Units with serial number 0606003 and higher are not included in this recall. MiniMax® NT Low NOx and MiniMax® NT TSI model pool heaters are not included in this recall.

CPSCJan 4, 2007Nationwide• Water Pool and Spa Inc., of Moorpark, Calif.

Spacelabs Healthcare, Incorporated: Ultraview SL Command Module with Masimo Sp02 Option, a mu...

Potential for modules to reset, alarms returning to default settings, invasive pressure losing its labels and zero calibration and Sp02 alarm limits being frozen. This can result in delay in treatment.

FDAJan 3, 2007Nationwide• Spacelabs Healthcare, Incorporated