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Terminated

Centurion Medical Products Port access tray with sorbaview 2000 and chloraprep DT9155, Sterile

FDA Recall Z-1090-2011 · Posted 2011-02-09

Recalling FirmCenturion Medical Products
Recall StatusTerminated
Product CodeLRS
Date Initiated2010-06-02
Date Terminated2011-02-09
Product Quantity100

Reason for Recall

The kits contain heparin lock flush solution USP code 504505 that is under recall by APP Pharmaceuticals. APP Pharmaceuticals is recalling the heparin because of incomplete documentation associated with test results.

Firm Action

Centurion Medical Products sent out Urgent Product Recall Notices on 6/3/2010. A second recall notice was sent to nonresponding consignees on 6/21/2010. The letter instructed the consignees to quarantine the recalled product and contact Centurion so that the recalled product can be retrieved.

Root Cause

Nonconforming Material/Component

Distribution Pattern

Nationwide distribution.

Official Source

View FDA Recall →

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

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