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Myriad Morcells™

AROA BIOSURGERY LIMITED · Model PW01NA0200 · UDI-DI 09421906017908

KGN Prescription
1
510(k) clearances
185
Adverse events (1 deaths)
23
Recalls
138
Facilities

Description

Myriad Morcells™ is derived from an extracellular matrix (ECM) composed of 100% w/w ovine (sheep) collagen.

Recalls

DateFirmReason
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-02-10Medline Industries, LPElevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.