PlainRecalls
FDA Devices Critical Class I Ongoing

SJM Pericardial Patch, with EnCap Technology 5x10 cm, Model Number REF C0510; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE

Reported: December 3, 2025 Initiated: October 9, 2025 #Z-0532-2026

Product Description

SJM Pericardial Patch, with EnCap Technology 5x10 cm, Model Number REF C0510; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE

Reason for Recall

The impacted lot may not meet the required tensile strength specification.

Details

Recalling Firm
Glycar SA Pty., Ltd.
Units Affected
18 units
Distribution
US
Location
Irene, N/A

Frequently Asked Questions

What product was recalled?
SJM Pericardial Patch, with EnCap Technology 5x10 cm, Model Number REF C0510; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE. Recalled by Glycar SA Pty., Ltd.. Units affected: 18 units.
Why was this product recalled?
The impacted lot may not meet the required tensile strength specification.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 3, 2025. Severity: Critical. Recall number: Z-0532-2026.