Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2059-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Bone Dowell Harvest Tubes

Product Classification:

Class II

Date Initiated: April 12, 2017

Date Posted: May 17, 2017

Recall Number: Z-2059-2017

Event ID: 77113

Reason for Recall:

mislabeled as 8mm tube but it is actually 9 mm in size. A 9mm subcomponent was erroneously substituted and etched as 8mm for the actual 8mm subcomponent part.

Status: Terminated

Product Quantity: 49

Code Information:

Part Number: 900738 Lot Number (LN): 889990

Distribution Pattern:

No US distribution. JAPAN NETHERLANDS SINGAPORE SWITZERLAND

Voluntary or Mandated:

Voluntary: Firm initiated