Z-0813-2007

BD 5ml Syringe Luer-Lok Tip Bulk Sterile Convenience Pak Latex Free

Name: Z-0813-2007 BD 5ml Syringe Luer-Lok Tip Bulk Sterile Convenience Pak Latex Free
Creator: Becton Dickinson & Company
Published: 2007-04-09
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2007-04-09 / Terminated / root cause: packaging

FDA source

Becton Dickinson & Company began a recall of BD 5ml Syringe Luer-Lok Tip Bulk Sterile Convenience Pak Latex Free on 2007-04-09. The reason FDA records is "Small cracks in plastic trays of one lot of BD 5mL Syringe Luer Lok Tip, Bulk Sterile Convenience Paks that may adversely affect tray integrity and steriity". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0813-2007
Status: Terminated
Initiated: 2007-04-09
Posted: 2007-05-24
Terminated: 2007-08-09
Recalling firm: Becton Dickinson & Co
Product: BD 5ml Syringe Luer-Lok Tip Bulk Sterile Convenience Pak Latex Free
Product code: FMF Syringe, Piston
Reason for recall: Small cracks in plastic trays of one lot of BD 5mL Syringe Luer Lok Tip, Bulk Sterile Convenience Paks that may adversely affect tray integrity and steriity.
Root cause tag: packaging
FDA root cause: Other
Action: Recall communications were sent on April 2, 2007 and May 3, 2007 by UPS second day air to all direct consignees and potential customers.
Quantity in commerce: 174,300 units
Distribution: Nationwide.
Product codes and lots: Lot number 7002604 Ref 309703

Product code FMF

K980987Class IIBecton Dickinson SyringeBd Becton Dickinson Vacutainer Systems Preanalytic / cleared 1998-06-11

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)