2005 Product Recalls

1,410 recalls issued in 2005.

1,410
Total Recalls
323
CPSC
441
FDA Device
646
NHTSA
CPSC 323 FDA Device 441 NHTSA 646

Showing 1401–1410 of 1,410 recalls

FDA

Magnetic Resonance Imaging System(s) Visart and Exelart P2/ Exelart P3/ Exelart SPIN and Exelart VANTAGE

Wrong positioning may cause patient burns.

An advisory letter will issue to all users May 26, 2004, with updated positioning information, and an employee will visit to make sure the letter was received and understood.

CPSC

Dirt Devil® Sweeper Vac™ Recalled for Fire Hazard

The vacuum's rotor can lock and overheat during use, causing a smoke and fire hazard.

Consumers should immediately stop using the product and contact Dirt Devil® to receive a free replacement.

FDA

Easypump LT 100-200 Elastomeric Infusion Pump (100 ml x 0.5 ml/hr) Part number: 5001120

Some pumps run at 2 ml/hr instead of 0.5 ml/hr.

Firm sent recall letter to thier only customer in France on August 23, 2002.

CPSC

Toddler Swings Recalled for Fall Hazard

The straps on these swings could break, causing a child riding in the swing to fall to the ground and suffer injuries.

Consumers should stop using these swings and contact the firm to determine if their swing is involved in the recall. If it is, the firm will provide a free repair.

FDA

Synchron Systems Acetaminophen Reagent, part No. 472169.

Firm shortened calibration frequency to 7 days from 14 days.

Firm issued letters to customers indicating need to shorten the calibration period from 14 to 7 days.

FDA

MicroSTAAR Injector w/ Foam Tip Plunger, Model MSI-PF

Injector mold design/manufacture and wear caused material flash to develop preventing assembly of the device prior to use.

Firm will be sending thier representatives to customers to inspect inventory and arrange return of product.

FDA

Vision Hollow Fiber Oxygenator with GBS Coating

Customers reported leakage.

Firm issued recall letters to all customers on March 4, 2004 listing lot numbers and quantities shipped to them. Returns were requested.

FDA

Collamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF

Risk of hyperopic refractive changes.

Firm is distributing letters to physicians suggesting ways to mitigate the observed contracture of the eye tissues after implantation. Letters will be sent 2/9/2004.

NHTSA

SEATS/GRA-MAG

A POSSIBLE VEHICLE CRASH COULD OCCUR SHOULD THE SEAT FALL BACKWARDS DURING USE.

DEALERS WILL REPAIR THESE VEHICLES. THE RECALL BEGAN ON APRIL 20, 2005. OWNERS MAY CONTACT FREIGHTLINER AT 1-800-547-0712.

NHTSA

HARLEY-DAVIDSON/REPLACEMENT FUEL VALVES

IF THE BIKE WERE OPERATING WITH THE VALVE IN THE 'ON' POSITION, THE BIKE COULD RUN OUT OF FUEL, THE EXPECTED FUEL RESERVE WILL NOT BE AVAILABLE. THIS COULD LEAD TO THE DRIVER RUNNING OUT OF GAS WITHOUT WARNING, INCREASING THE RISK OF A CRASH.

DEALERS WILL INSPECT THE FUEL VALVE AND REPLACE IT, IF NECESSARY. THE RECALL BEGAN JANUARY 27, 2005. OWNERS SHOULD CONTACT HARLEY-DAVIDSON AT 1-414-342-4080. IF YOU HAVE HAD OR INSTALLED A REPLACEMENT FUEL SHUT-OFF VALVE IN YOUR MOTORCYCLE, PLEASE TAKE YOUR VEHICLE TO YOUR DEALER TO HAVE THE VALVE INSPECTED FOR PROPER OPERATION AS SOON AS POSSIBLE.