Stryker Sustainability Solutions: Medical Device Recall in 2024 - (Recall #: Z-2405-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly

Product Classification:

Class II

Date Initiated: May 31, 2024

Date Posted: July 24, 2024

Recall Number: Z-2405-2024

Event ID: 94824

Reason for Recall:

Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.

Status: Ongoing

Product Quantity: 90 units

Code Information:

Lot: 0000564862/ UDI: 00885825015411

Distribution Pattern:

US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.

Voluntary or Mandated:

Voluntary: Firm initiated