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Terminated

BD 20 ml Syringe Luer-Lok Tip Sterile, Do not reuse; Catalog Number 309661.

FDA Recall Z-1488-2009 · Posted 2009-06-24

Recalling FirmBecton Dickinson & Company
Recall StatusTerminated
Product CodeFMF
Date Initiated2009-04-30
Date Terminated2009-09-28
Product Quantity201,600 units

Reason for Recall

Potential for compromised sterility: Insufficient packaging seals.

Firm Action

Becton Dickinson sent Urgent Product Recall letters on April 30, 2009 to all direct customers. Questions are to be directed to BD Customer Service at 1-888-237-2762. Letters to customers of distributors went out on May 12, 2009.

Root Cause

Nonconforming Material/Component

Distribution Pattern

Nationwide Distribution.

Official Source

View FDA Recall →

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

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