STERILMED, INC.: Medical Device Recall in 2015 - (Recall #: Z-2819-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown (PLC), 34", Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed. Products are individually packaged in a Tyvek¿/poly pouch. There are 5 pouches placed inside a casepack box. Each sales unit (casepack) contains 5 devices.

Product Classification:

Class II

Date Initiated: August 24, 2015

Date Posted: October 7, 2015

Recall Number: Z-2819-2015

Event ID: 72035

Reason for Recall:

Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part #ZIM60-7075-106, lot number 1846885 due to mislabeling. The affected reprocessed product is labeled as single hose devices but the devices inside the packaging are dual hose devices.

Status: Terminated

Product Quantity: 43

Code Information:

Lot 1846885

Distribution Pattern:

US Nationwide Distribution in the states of CA, KY, MI, OH, UT and WI.

Voluntary or Mandated:

Voluntary: Firm initiated