Please read all of the information below carefully
Dear Valued Customer,
We hope this message finds you well. We are writing to inform you of an urgent recall
concerning the Stryker products that you have received from St John Supplies.
This recall is due to a critical issue identified during the manufacturing process. Please read the full email to find out what actions must be taken. The device recall notification can be downloaded here.
Details of the Affected Products:
Product Name: HeartSine Samaritan PAD Automated External Defibrillator
Product Codes and Lot Numbers:
SAM 350P
SAM 360P
SAM 450P
SAM 500P
Reason for Recall:
It was determined during extensive quality testing that a manufacturing process issue related to a circuit board component may impair the device’s ability to function or cause failure. This failure could occur at any point when the device is holding a charge in preparation to deliver therapy, while delivering a shock, or after shock delivery. The device becomes inoperable after the failure occurs.
Actions Required:
Identify and Quarantine: Immediately identify and quarantine any potentially affected products from the lot numbers listed above.
Complete the Reply Form: Please complete the attached Reply Form to confirm the products you have identified and to arrange for their collection and credit.
Confirm No Affected Devices: If you do not have any affected devices in stock, please confirm this using the Reply Form.
Return the Reply Form: Send the completed Reply Form to nby_qara@stryker.com to confirm receipt of this notice and that the necessary actions have been taken.
Deadline for Action:
Please complete these actions immediately upon receipt of this notice and continue until no affected stock remains. The deadline for returning the customer reply form is 31/07/2025.
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