HomeMedical Device recalls
High severity

SJM Pericardial Patch, with EnCap Technology 9x14cm, Model Number REF C0914; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE

SourceFDA Device Enforcement
CategoryMedical Device
SeverityHigh
Statusongoing
Recall dateOctober 09, 2025
ReportedDecember 03, 2025
Recalling firmGlycar SA Pty., Ltd.
Country / regionSouth Africa N/A

Hazard

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

Affected products

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