Stryker Sustainability Solutions: Medical Device Recall in 2020 - (Recall #: Z-1802-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868, Reprocessed Tourniquet Cuff - Product Usage: Reprocessed tourniquet cuffs are indicated for use in patients who require surgery of the extremities with an expected duration of less than 90 minutes when temporary exsanguination of a limb is desired.

Product Classification:

Class II

Date Initiated: October 9, 2019

Date Posted: May 6, 2020

Recall Number: Z-1802-2020

Event ID: 85330

Reason for Recall:

Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadequate Limb Compression Force.

Status: Terminated

Product Quantity: 90

Code Information:

Lot Number 10237165

Distribution Pattern:

US Nationwide distribution including the states of SC, TX, UT, NY, AR

Voluntary or Mandated:

Voluntary: Firm initiated