HeartSine Samaritan PAD recall
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Why was HeartSine Samaritan PAD recalled?
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN/UDI: 05060167120695, Serial Number: 20D00009694
- Product
- HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
- Recalling firm
- Physio-Control, Inc.
- Quantity
- 1
- Distribution
- U.S.: AK
- Recall date
- March 16, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)