The Recall Desk
HighFDA (Devices)·Z-0392-2022·Announced 2021-12-29

Stryker CLAW II ORTHOLOC 3DSi Plate Recall: Incorrect Product in Packaging

Wright Medical Technology is recalling Stryker CLAW II ORTHOLOC 3DSi Plates due to incorrect products being contained in packaging.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is a Class II medical device recall involving an orthopedic implant where incorrect products were packaged. The replacement of the correct surgical implant with an incorrect product represents a risk-of-harm situation, even though no illnesses or injuries have been reported.

Plain-English summary

Wright Medical Technology Inc is recalling the Stryker CLAW II ORTHOLOC 3DSi Plate (Hole Qty: 4, 30mm, REF 40240430, Lot #1642103). The recall was initiated because the incorrect product is contained in the packaging.

The affected product was distributed worldwide. In the United States, distribution occurred in Arizona, Iowa, Idaho, North Carolina, New York, Virginia, and West Virginia. Internationally, the product was distributed to Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and the United Kingdom. A total of 23 units are involved in this recall.

The recalled product

Product
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Manufacturer
Wright Medical Technology Inc
Category
Medical Device — Orthopedic Implant
Hazard
  • packaging-error

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot #1642103

Distribution

Distributed in 7 states:

  • AZ
  • IA
  • ID
  • NC
  • NY
  • VA
  • WV

Related recalls

Same category