Stryker GmbH: Medical Device Recall in 2018 - (Recall #: Z-1526-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults.

Product Classification:

Class II

Date Initiated: March 12, 2018

Date Posted: May 2, 2018

Recall Number: Z-1526-2018

Event ID: 79751

Reason for Recall:

The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling

Status: Terminated

Product Quantity: 18

Code Information:

Lot # L23745

Distribution Pattern:

USA (nationwide) Distribution

Voluntary or Mandated:

Voluntary: Firm initiated