Physio-Control, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0745-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak

Product Classification:

Class III

Date Initiated: January 13, 2022

Date Posted: March 16, 2022

Recall Number: Z-0745-2022

Event ID: 89536

Reason for Recall:

Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.

Status: Terminated

Product Quantity: 1

Code Information:

GTIN/UDI: 05060167120695, Serial Number: 20D00009694

Distribution Pattern:

U.S.: AK

Voluntary or Mandated:

Voluntary: Firm initiated