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Terminated

Portex Hypodermic Needle-Pro Syringe & Needle 3mL/LL 25G x1'' Catalog Number: 4238

FDA Recall Z-0858-05 · Posted 2005-06-01

Recalling FirmSmiths Medical ASD, Inc.
Recall StatusTerminated
Product CodeFMI
Date Initiated2005-05-05
Date Terminated2012-05-08
Product Quantity159 cases (400 per case) =63,600 each.

Reason for Recall

Mislabeled: Product may contain an incorrect needle size. Product labeled as a 25G x 1" may contain a 25G x 5/8"

Firm Action

Smith Medical notified dealers of the recall on May 5, 2005 by telephone. The remaining customers were notified on May 12, 2005 by telephone. Follow-up letter delivered by Federal Express on May 17, 2005.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

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

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