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Terminated

MMP 200 Articulating Booms, Catalog Number 0682-000-604SX, Product Number 0682-001-060C. Used for operating room equipment.

FDA Recall Z-1611-2011 · Posted 2011-03-08

Recalling FirmStryker Communications Corp
Recall StatusTerminated
Date Initiated2011-01-28
Date Terminated2011-03-30
Product Quantity2

Reason for Recall

Utilization of incorrect screws resulted in inadequate thread engagement reducing the load bearing capability of the product.

Firm Action

Stryker notified consignees verbally on January 28, 2011 and by letter dated February 11, 2011.

Root Cause

Process control

Distribution Pattern

MA, CO

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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