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Showing 86841–86860 of 92420 results

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Stryker Howmedica Osteonics Corp.: Citation AT Femoral Stem

The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.

FDAAug 24, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Hamilton Co: Y-valve and T-valve, PSD/4 Syringe Drive Module parts.

The product valve has a high probability of deforming and may result in leakage during use.

FDAAug 24, 2005CA, IN, MA +2 more• Hamilton Co

Stryker Howmedica Osteonics Corp.: Reliance PF Femoral Stem

The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.

FDAAug 24, 2005Nationwide• Stryker Howmedica Osteonics Corp.

ZoloWear Infant Carriers (ZoloWear) – Fabric Safety Concern (2005)

The recalled slings are made of 100-percent cotton fabric or 97 percent cotton/ 3 percent Lycra with two pieces of webbing holding the rings to the fabric. Solid natural color and five prints (Splash, Pink and Black Stripe, Pink and Brown Stripe, Pink Punch and The Hamptons) make up the lots included in the recall. A large white label sewn on the pocket of the slings reads "Zolo." ZoloWear slings should have three rows of stitching securing the webbing and fabric together. Some of the slings in these lots have short webbing, so only one row of stitching holds the webbing in place.

CPSCAug 23, 2005Nationwide• ZoloWear Inc., of Austin, Texas

Tiki® Bamboo Torches (Lamplight Farms) – Potential Fire Risk (2005)

These 5-foot-tall Tiki® bamboo torches consist of a bamboo pole with a weaved basket at the top and a metal flame guard, which is a circular black piece that holds the wick in place and attaches to the fuel canister. The recall includes the Tiki® Beachcomber, Seagrass and Sandpiper model torches. The recall also involves replacement canisters that have the metal flame guards. Recalled units have the following UPC numbers: 086861010372 (Beachcomber), 086861013335 (Seagrass), 086861010457 (Sandpiper) and 076354995262 (Replacement Canister). The UPC number and the model name are written on the packaging or attached tag.

CPSCAug 23, 2005Nationwide• Lamplight Farms Inc., of Menomonee Falls, Wis.

Stryker Endoscopy: Biosteon brand HA/PLLA Cross Pin, Model Number 234-500-3...

The medical device is misbranded in that the package is labeled as Biosteon Interference Screw in fact contains Biosteon Cross Pin. This mislabeling could disrupt surgery preparation resulting in surgery delay.

FDAAug 23, 2005OR, VA• Stryker Endoscopy

Zimmer Inc.: Zimmer brand Bigliani/Flatow Total Shoulder trabecular me...

The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement.

FDAAug 23, 2005Nationwide• Zimmer Inc.

St. Jude Medical Daig Division: Angio-Seal Vascular Closure Device. Ref 610109. 6F STS ...

Mispackaging-Some Angio-Seal 6F STS Vascular Closure Devices from Lot no. 1146548 have been incorrectly packaged with a 0.035' guidewire instead of a 0.032' guidewire.

FDAAug 22, 2005Nationwide• St. Jude Medical Daig Division

Coffeemaker Carafe (West Bend) – Potential Defect (2005)

The carafe is a 10-cup capacity glass pot with a black, plastic handle. It is used with the West Bend Housewares 10-cup Automatic Coffeemaker (item # 56870). The 10-cup replacement carafe was sold separately (item # 5815). There is a four-digit date code printed on the bottom of the coffeemaker. Date codes beginning with 04 are included in this recall.

CPSCAug 19, 2005Nationwide

Stork Craft Toy Boxes (Stork Craft) – Manufacturing Flaw (2005)

The recall includes toy boxes with manufacture date codes between November 2002 and July 2004 and the following model numbers and colors: 01520-331 - white, 01520-334 - cherry, 01520-33C - cognac, 01520-33L - oak, and 01520-33N - natural. The manufacture date codes, model numbers, and colors are located on a label underneath the toy boxes. The toy boxes measure 27 inches long by 18 inches wide and 17 inches high. The boxes are constructed of pine.

CPSCAug 19, 2005Nationwide• Stork Craft Manufacturing Inc., of Richmond, British Columbia, Canada

BIOMERIEUX, INC.: VeriCal Calibrator Set

The product is being recalled due to mis-assignment of ISI values associated with VeriCal use.

FDAAug 19, 2005Nationwide• BIOMERIEUX, INC.

GE Medical Systems, LLC: GE Signa Advantage nuclear magnetic resonance imaging sys...

During use of GE Signa nuclear magnetic resonance imaging system, a flexible Teflon tube that was part of the magnet vent system ruptured and allowed the magnet to vent into the scan room. Because of helium pressure inside the room, the scan room door could not be reopened after the patient was removed from the scan room.

FDAAug 19, 2005Nationwide• GE Medical Systems, LLC

Datascope Corp: Panorama Patient Monitoring Network, Cardiac Arrhythmia M...

The software version contains an anomaly which could freeze the unit when the right click button is used on the mouse.

FDAAug 19, 2005Nationwide• Datascope Corp

GeoDeck™ Decking (Kadant Composites) – Material Safety Issue (2005)

Laceration Risk

GeoDeck™ is a composite decking product that looks similar to natural wood and is sold in three colors, including: driftwood, cedar and mahogany. The decking materials were manufactured between April 2002 and October 2003. Each decking and railing component has a manufacturing date stamp (day/month/year) on the cut end, which may still be visible on uninstalled materials.

CPSCAug 19, 2005Nationwide• Kadant Composites Inc., of Bedford, Mass.

Chelsea Pub Stool (Unknown) – Structural Integrity (2005)

The stool is marketed under the brand name of GardenWood Furniture. The recalled pub stools include the Chelsea Pub Stools model numbers 986W and 986KFRS, as indicated on the outside of the box. Both stools are constructed with wood legs, seats, and back-rests. Seat height is 30 inches and was sold both unfinished (W) as well as in a clear, penetrating oil finish (KFRS). Units with Lot code #06222005 are not affected by this recall.

CPSCAug 18, 2005Nationwide

Tosoh Bioscience, Inc.: Tosoh brand Glycohemoglobin A1c Controls I & II, Catalog ...

The firm has received reports that vials of the Level II were exhibiting poor and inconsistent chromatogram quality thus affecting control results.

FDAAug 18, 2005PR• Tosoh Bioscience, Inc.

Philips Medical Systems (Cleveland) Inc: Gemini GXL PET/CT Systems, 6, 10, 16 slice configurations...

The image balance center point correction algorithm used in CT image reconstruction may cause a disapperance or alteration of small circular anatomical structures that are both near the image center and perpendicular to the image plane. This artifact may lead to the misinterpretation of anatomy at the center of the image.

FDAAug 18, 2005IN• Philips Medical Systems (Cleveland) Inc

Water Watch (Unknown) – Liquid Containment Risk (2005)

The watches are made of clear plastic with white snaps. The watch bands have clear glitter-filled liquid and colored liquid inside including pink, blue, red and yellow. The watch face is digital and measures about two inches in width. "Water Watch" and "Almar Sales Company" is printed on the original clear bubble packaging of the watches.

CPSCAug 17, 2005Nationwide

Bicycle Tires (Torelli Imports) – Potential Rim Failure (2005)

This recall involves Torelli Verona and Lugano Open Tubular bicycle tires with folding Kevlar beads, used to hold the tire to the rim. A red and white label on the sidewall of the Verona model has "Torelli Verona 700 X 23 100-130 psi Handmade Open Tubular" printed on it. A green and white label on the lower edge of the Lugano model has "Torelli Lugano 700 X 23 100-130 psi Handmade Open Tubular" printed on it. The tires are packaged in red and white boxes with the Torelli logo on the front.

CPSCAug 17, 2005Nationwide• Torelli Imports, of Camarillo, Calif.

C.R. Bard, Inc., Urological Division: Bard * Davol Reliavac 400 Closed Wound Suction Kit * Ster...

An incorrect Y-connector was placed in the kit.

FDAAug 17, 2005AL, CA, FL +6 more• C.R. Bard, Inc., Urological Division

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