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Terminated

Applied Blunt Tip Trocar Models C0717 and C0718

FDA Recall Z-0009-05 · Posted 2004-10-05

Recalling FirmApplied Medical Resources Corp
Recall StatusTerminated
Product CodeKXN
Date Initiated2004-09-17
Date Terminated2005-08-05
Product Quantity1025

Reason for Recall

Inadequate trocar tip assembly that might yeild parts to patients.

Firm Action

Initiated recall by letter on 9/16/2004 via Fedex/UPS. Follow-up to nonresponders in 30 days.

Root Cause

Other

Distribution Pattern

Nationwide. Ireland.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K923636TROCAR W/ BLUNT TIP OBTURATORApplied Medical Resources · 1993-11-05

Official Source

View FDA Recall →

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

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