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Terminated

Arrow Continuous Nerve Block Needle, Latex-Free* Rx only*Sterile*Arrow International Inc., 2400 Bernville, Road, Reading, PA 19605 USA

FDA Recall Z-0852-05 · Posted 2005-06-01

Recalling FirmArrow International Inc
Recall StatusTerminated
Product CodeCAZ
Date Initiated2005-02-17
Date Terminated2006-05-05

Reason for Recall

Possible difficulty in passing the catheter through the needle due to a reduced ID of the needle caused by over crimping of the needle during the manufacturing process.

Firm Action

Consignees were notifed by letter on/about 02/17/2005

Root Cause

Other

Distribution Pattern

Nationwide, Africa , France, Holland, Rotterdam

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K021567STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000Arrow Intl., Inc. · 2002-06-19

Official Source

View FDA Recall →

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

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