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Terminated

BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder.

FDA Recall Z-0372-06 · Posted 2006-01-11

Recall StatusTerminated
Product CodeKSR
Date Initiated2005-12-01
Date Terminated2007-04-30
Product Quantity118200 each

Reason for Recall

Cracked finger grip luer adapter components on the Push Button Blood Collection Set.

Firm Action

Recall notification was sent out to the customers on 12/5/2005.

Root Cause

Other

Distribution Pattern

The device was shipped to 23 wholesalers, 5 hospitals, and 1 VA govt. account nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

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

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