Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2018 - (Recall #: Z-0419-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

MA3320-PM Premium Adult - SYK Mistral-Air Premium Blankets. MODEL #: MA3302-PM. CATALOG #(s): MA3302-PM

Product Classification:

Class II

Date Initiated: July 21, 2017

Date Posted: February 7, 2018

Recall Number: Z-0419-2018

Event ID: 78886

Reason for Recall:

It was identified that the Mistral-Air Premium blankets may be capable of conducting electricity during a defibrillation or cardioversion therapy at higher energy levels (70 Joules or more) when the blanket is applied with the reflective side toward the patient (upside down).

Status: Terminated

Product Quantity: 11160

Code Information:

LOT #(s): 1640002, 1645003

Distribution Pattern:

U.S.

Voluntary or Mandated:

Voluntary: Firm initiated