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Terminated

Angiographic Syringe, 12 cc Thumb Ring with Rotator Reservoir.

FDA Recall Z-0618-05 · Posted 2005-03-15

Recalling FirmHospira Inc.
Recall StatusTerminated
Product CodeDQO
Date Initiated2004-11-02
Date Terminated2005-07-25
Product Quantity8175 syringes

Reason for Recall

Syringes could possibly allow air to enter the patient's vascular system.

Firm Action

Consignees were notified by letter on 11/10/04 or by telephone on 11/11/04.

Root Cause

Other

Distribution Pattern

Domestic distribution: Nationwide, including 2 military/VA facilities. International distribution: Spain, Belgium, Greece, Japan, and France.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K942329HAND CONTROLLED SYRINGEAbbott Laboratories · 1994-06-20K933700DYE MANAGEMENT SYSTEMAbbott Laboratories · 1993-11-03K932188SAFESET RESERVOIRAbbott Laboratories · 1993-10-25K884823TRANSPAC(R) II, DISPOSABLE TRANSDUCERAbbott Laboratories · 1990-07-03

Official Source

View FDA Recall →

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

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