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Terminated

BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications

FDA Recall Z-1009-2012 · Posted 2012-02-13

Recalling FirmBecton Dickinson & Company
Recall StatusTerminated
Product CodeFMI
Date Initiated2011-10-08
Date Terminated2012-12-11
Product Quantity480,000 units

Reason for Recall

Becton Dickinson has identified clogged needles.

Firm Action

Becton Dickinson sent Urgent Product Recall letters dated October 18, 2011 and October 17, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to check their inventory to deterine if they have any of the affected product. If they have affected product customers should return the product to Beckton Dickinson. For any questions regarding this recall call 201-847-4344.

Root Cause

Device Design

Distribution Pattern

Nationwide Distribution including IL and NJ

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K021475BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SETBd · 2002-07-19

Official Source

View FDA Recall →

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

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