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DELTA

Stryker Leibinger GmbH & Co. KG · Model 70-06350 · UDI-DI 04546540337337

GXR HBW JEY MAI Prescription

510(k) clearances

210

Adverse events

Recalls

Facilities

Description

DELTA 2.2MM MESH 55X55X1.4MM

Recalls

Date	Firm	Reason
2021-06-02	Medtronic Neuromodulation	Excess nylon flash on the clip.

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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.