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Terminated

50 mL sterile plastic centerfuge tubes.

FDA Recall Z-0512-04 · Posted 2004-02-04

Recalling FirmStockwell Scientific Inc
Recall StatusTerminated
Product CodeJKA
Date Initiated2003-12-29
Date Terminated2004-04-08
Product Quantity3762 cases (500 tubes/cs)

Reason for Recall

Tubes are brittle and break during centerfuging specimens.

Firm Action

Firm sent a recall letter to all customers 12/30/2003 requesting return of existing stock and subrecall of subdistributed product.

Root Cause

Other

Distribution Pattern

Nationwide and Canada

Official Source

View FDA Recall →

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

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