Z-0372-06

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

Name: Z-0372-06 BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder
Creator: Becton Dickinson & Company
Published: 2005-12-01
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2005-12-01 / Terminated

FDA source

Becton Dickinson & Company began a recall of BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder on 2005-12-01. The reason FDA records is "Cracked finger grip luer adapter components on the Push Button Blood Collection Set". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0372-06
Status: Terminated
Initiated: 2005-12-01
Posted: 2006-01-11
Terminated: 2007-04-30
Recalling firm: Becton Dickinson & Co
Product: BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder.
Product code: KSR Container, Empty, For Collection & Processing Of Blood & Blood Components
Reason for recall: Cracked finger grip luer adapter components on the Push Button Blood Collection Set.
FDA root cause: Other
Action: Recall notification was sent out to the customers on 12/5/2005.
Quantity in commerce: 118200 each
Distribution: The device was shipped to 23 wholesalers, 5 hospitals, and 1 VA govt. account nationwide.
Product codes and lots: Catalog # -- Lot #: 367352 -- 5188576; 367352 -- 5208448; 367352 -- 5217290; 368656 -- 5164491; 368656 -- 5164526; 368656 -- 5187894; 368656 -- 5192496; 368656 -- 5220204; 368656 -- 5238936.

Product code KSR

K011984Class IIBd Vacutainer Push Button Blood Colection SetBecton, Dickinson & CO / cleared 2001-08-29

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)