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Terminated

Pencil Point Spinal Tray, Lot number 0504243

FDA Recall Z-1114-04 · Posted 2004-07-20

Recalling FirmSpinal Specialties, Inc
Recall StatusTerminated
Product CodeLRO
Date Initiated2004-06-18
Date Terminated2004-10-20
Product Quantity20 units

Reason for Recall

Kit contains lidocaine, which has particulate matter in its ampule.

Firm Action

Firm notified consignees who received the product by telephone on 6/18/2004, then sent a letter via facsimile and next day air delivery.

Root Cause

Other

Distribution Pattern

El Paso, Texas and Lansing, Michigan

Official Source

View FDA Recall →

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

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