Zimmer Surgical Inc: Medical Device Recall in 2020 - (Recall #: Z-1356-2020)

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 Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No. 60708015200, UDI (01)00889024377547 (17)230812(10)27968701 The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field.

Product Classification:

Class II

Date Initiated: January 3, 2020

Date Posted: March 4, 2020

Recall Number: Z-1356-2020

Event ID: 84752

Reason for Recall:

When inflating/deflating a single bladder, both bladders could potentially inflate/deflate due to a leak between the bladders.

Status: Terminated

Product Quantity: 58

Code Information:

Lot 27968701

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of CA, FL, IA, ID, IL, LA, MA, MO, NC, NY, OH, OR, PA, SC, TN, TX, WA, WI, and WV and country of Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated