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Recall Observatory FDA recall evidence

Device product

Product 4 consists of all products under product code HWC, and same usage: Item no: 47482002603 2.0 X 26 CORT SCREW CRUCI 47482002803 2.0 X 28 CORT SCREW CRUCI 47482003203 2.0 X 32 CORT SCREW CRUCI 47482003403 2.0 X 34 CORT SCREW CRUCI 47482003603 2.0 X 36 CORT SCREW CRUCI 47482003803 2.0 X 38 CORT SCREW CRUCI 47482004003 2.0 X 40 CORT SCREW CRUCI 47482004203 2.0 X 42 CORT SCREW CRUCI 47482004403 2.0 X 44 CORT SCREW CRUCI 47482004603 2.0 X 46 CORT SCREW CRUCI 47482004803 2.0 X 48 CORT SCREW CRUCI 47482005003 2.0 X 50 CORT SCREW CRUCI 47482702000 2.7 X 20 CORT SCREW HEX Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.

Z-1102-2016

January 11, 2016

Class II

Product summary

Firm
Zimmer Manufacturing B.V.
Event
Event 72900
Status
Terminated
Classification
Class II
Quantity
154
Official record key
device-enforcement:Z-1102-2016

Official wording

Reason: As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.

Code information: lot no.61951256 62230459 61907760 61907764 61926199 62261661 61926201 61907767 61907769 61907771 61909381 62230462 61907772 61196133 61907773 62020888 61920808

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.