Stryker Sustainability Solutions: Medical Device Recall in 2023 - (Recall #: Z-1612-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile

Product Classification:

Class II

Date Initiated: April 14, 2023

Date Posted: May 24, 2023

Recall Number: Z-1612-2023

Event ID: 92138

Reason for Recall:

Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be mislabeled and/or mispackaged.

Status: Ongoing

Product Quantity: 50 units

Code Information:

Lot # 0000157564, UDI-DI: 00885825013585

Distribution Pattern:

US: WA OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated