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Terminated

Kendall MONOJECT MAGELLAN SAFETY NEEDLE 21G X 1 inch Product Number: 5551850115

FDA Recall Z-0104-05 · Posted 2004-11-02

Recalling FirmKendall Healthcare Products Co
Recall StatusTerminated
Product CodeFMI
Date Initiated2004-10-08
Date Terminated2012-05-15

Reason for Recall

Needle cannula may separate from the hub during use

Firm Action

Recall letters requesting product return were mailed to all customers on October 8, 2004

Root Cause

Other

Distribution Pattern

Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K012736MONOJECT SAFETY NEEDLETyco Healthcare · 2001-10-25

Official Source

View FDA Recall →

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

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