SJM Pericardial Patch, with EnCap Technology 5x10 cm, Model Number REF C0510; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE
FDA Recall Z-0532-2026 · Posted 2025-11-25
Advertisement
Recalling FirmGlycar SA Pty., Ltd.
Recall StatusOpen, Classified
Product CodeDXZ
Date Initiated2025-10-09
Product Quantity18 units
Reason for Recall
The impacted lot may not meet the required tensile strength specification.
Firm Action
Glycar issued a Stock Withdrawal Notification to its sole distributor on 10/09/2025. The notice explained the issue and requested the following:
"Required Actions
1. Immediately identify and segregate all affected stock in your possession.
2. Clearly label the identified stock as "WITHDRAWN PRODUCT" DO NOT DISTRIBUTE OR USE.
3. Suspend any further distribution or transfer of the affected lots. 4. Provide written confirmation of the quantity and storage location of all affected stock within five (5) business days of receipt of this notification.
5. Our Quality team will coordinate collection, return, or replacement of affected product as appropriate."
For questions or require further clarification, contact: Malcolm Applewhite, [email protected]
On 10/17/2025, the firm issued an URGENT: MEDICAL DEVICE RECALL notice the medical facility via email. This notice explained the issue, potential risk to health, and requested the following:
"Actions to be Taken by the Customer / User:
1. Identify and quarantine any affected products with lot number T2502257 in your possession.
2. Cease use of the affected device immediately.
3. Share this notice with applicable personnel within your institution.
4. Abbott will coordinate and arrange for return and replacement of affected units.
5. Complete and return the attached Acknowledgment Form within 5 business days to confirm receipt of this notice."
For questions or assistance, contact: Regulatory Affairs Manager, Glycar SA (Pty) Ltd, Malcolm Applewhite, [email protected]
Root Cause
Process control
Distribution Pattern
US
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement