Z-0619-05

Angiographic Syringe, 12 cc Thumb Ring with Rotator Non-Reservoir

Name: Z-0619-05 Angiographic Syringe, 12 cc Thumb Ring with Rotator Non-Reservoir
Creator: Hospira Inc.
Published: 2004-11-02
License: https://open.fda.gov/license/

Abbott Medical / initiated 2004-11-02 / Terminated

FDA source

Hospira Inc. began a recall of Angiographic Syringe, 12 cc Thumb Ring with Rotator Non-Reservoir on 2004-11-02. The reason FDA records is "Syringes could possibly allow air to enter the patient's vascular system". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0619-05
Status: Terminated
Initiated: 2004-11-02
Posted: 2005-03-15
Terminated: 2005-07-25
Recalling firm: Abbott Medical
Product: Angiographic Syringe, 12 cc Thumb Ring with Rotator Non-Reservoir.
Product code: DQO Catheter, Intravascular, Diagnostic
Reason for recall: Syringes could possibly allow air to enter the patient's vascular system.
FDA root cause: Other
Action: Consignees were notified by letter on 11/10/04 or by telephone on 11/11/04.
Quantity in commerce: 250 syringes
Distribution: Domestic distribution: Nationwide, including 2 military/VA facilities. International distribution: Spain, Belgium, Greece, Japan, and France.
Product codes and lots: List Numbers: 4204401 Lot Numbers: 17149SN

Product code DQO

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)