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Terminated

BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950.

FDA Recall Z-1525-06 · Posted 2006-09-28

Recalling FirmBecton Dickinson & Company
Recall StatusTerminated
Product CodeMEG
Date Initiated2006-07-24
Date Terminated2007-12-03
Product Quantity1,294,200 units

Reason for Recall

BD received reports of needle assembly disengagement from the syringe.

Firm Action

Recall letters were sent to all wholesalers and end users on 7/28/2006.

Root Cause

Other

Distribution Pattern

Nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K992734BECTON DICKINSON SYRINGEBd Becton Dickinson Vacutainer Systems Preanalytic · 1999-10-01

Official Source

View FDA Recall →

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

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