Straumann Manufacturing, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2534-2016)

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:

Straumann Bone Level Implant, ¿ 4.1mm RC, SLA 10mm, TiZr, NTP Article Number: 021.4510

Product Classification:

Class II

Date Initiated: July 14, 2016

Date Posted: August 24, 2016

Recall Number: Z-2534-2016

Event ID: 74799

Reason for Recall:

Misalignment with the Loxim transfer piece markings, the positioning of the implant will be incorrect for optimal restoration

Status: Terminated

Product Quantity: 70 pieces

Code Information:

Lot Numbers: LR810; LT122

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated