Physio-Control, Inc. HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Brand
Physio-Control, Inc.
Lot Codes / Batch Numbers
GTIN/UDI: 05060167120695, Serial Number: 20D00009694
Products Sold
GTIN/UDI: 05060167120695, Serial Number: 20D00009694
Physio-Control, Inc. is recalling HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak due to Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
Recommended Action
Per FDA guidance
On 01/13/2022, Stryker telephoned the customer and informed them of the correction. The telephone call was followed up with a correction notice, mailed to the customer on 01/17/22, that informed the customer to contact Customer Service at 1 800 787 9537, option 2, 8:00 A.M. to 7:00 P.M. (Eastern Time), Monday - Friday or by email at medtechsup@stryker.com if they had questions or concerns.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AK
Page updated: Jan 10, 2026