Implant Direct Sybron Manufacturing, LLC: Medical Device Recall in 2016 - (Recall #: Z-2320-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

RePlant¿ Angled Abutment Part Number 6050-52-60

Product Classification:

Class II

Date Initiated: July 5, 2016

Date Posted: August 10, 2016

Recall Number: Z-2320-2016

Event ID: 74624

Reason for Recall:

Issue with design specification; oversized condition.

Status: Terminated

Product Quantity: 205

Code Information:

Lot #50174, 39799, 49364

Distribution Pattern:

U.S. distribution to the following; CA, WA, UT, GA, AZ, NE, OR, MI, TX, WI, FL, AL, AR, MO, VA, MA, TN, LA, NC, KS, NY, SC, OK. Foreign distribution to the following; CA, DE, IT, GB, PL, DE, GB, NL, GR, ES, HR, BG.

Voluntary or Mandated:

Voluntary: Firm initiated