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MTI

Medical Technology Industries, Inc. · Model 330-01-216 · UDI-DI 10840118422366

FZM

510(k) clearances

392

Adverse events

Recalls

Facilities

Description

Stool, Hydraulic Pump w/Body Support w/TB133, PREMIUM-PINE FOREST

Recalls

Date	Firm	Reason
2021-05-12	Stryker Medical Division of Stryker Corporation	Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden

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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.