Synthes USA HQ, Inc.: Medical Device Recall in 2013 - (Recall #: Z-2087-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Synthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H HD/3H Shaft/Right Product Usage: Intended for fixation of complex intra-and extra-articular fractures and osteotomies of the distal radius and other small bones.

Product Classification:

Class II

Date Initiated: July 30, 2013

Date Posted: September 4, 2013

Recall Number: Z-2087-2013

Event ID: 65890

Reason for Recall:

The possibility exists that 2.4 mm VA-LCP 2 column distal radius plates from a specific lot are etched with "R" for right plate when they should be etched with "L" for left plate.

Status: Terminated

Product Quantity: 11

Code Information:

Part No. 02.111.730, with Lot No. 3614792

Distribution Pattern:

USA Nationwide Distribution in the states of FL, GA, NC, OH, KY, NJ, ID, IN, and MN.

Voluntary or Mandated:

Voluntary: Firm initiated