Z-0915-2008

BD 10 ml Syringe Luer Lok Tip, Reorder #3039605, BD, Franklin Lakes, NJ 07417

Name: Z-0915-2008 BD 10 ml Syringe Luer Lok Tip, Reorder #3039605, BD, Franklin Lakes, NJ 07417
Creator: Becton Dickinson & Company
Published: 2008-01-07
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2008-01-07 / Terminated / root cause: packaging

FDA source

Becton Dickinson & Company began a recall of BD 10 ml Syringe Luer Lok Tip, Reorder #3039605, BD, Franklin Lakes, NJ 07417 on 2008-01-07. The reason FDA records is "Defective Seal: The convenience trays may have open seals, which can adversely impact tray sterility". 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-0915-2008
Status: Terminated
Initiated: 2008-01-07
Posted: 2008-04-16
Terminated: 2008-05-19
Recalling firm: Becton Dickinson & Co
Product: BD 10 ml Syringe Luer Lok Tip, Reorder #3039605, BD, Franklin Lakes, NJ 07417.
Product code: FMF Syringe, Piston
Reason for recall: Defective Seal: The convenience trays may have open seals, which can adversely impact tray sterility.
Root cause tag: packaging
FDA root cause: Packaging
Action: BD notified distributors by an Urgent Product Recall Letter sent via UPS on January 7, 2008. In addition, the firm sent an Urgent Product Recall Letter on January 11, 2008 to customers identified by the distributors. The letter instructed the users to remove the product from its inventory and to return affected products to the firm using an enclosed customer packing list. For additional information, contact 1-888-237-2762.
Quantity in commerce: 2,926,560
Distribution: Nationwide, including the states of CA, NY, MO, MA, IL, OH, TN, TX, MI, LA, MO, ID, GA, NE, SC and FL.
Product codes and lots: Reorder number: 3039605; Lot numbers 7061015, 7061014, 7092726, 7094789, 7094790, 7123223, 7123225, 7150947, 7150949, 7184442, 7184443, 7184446, 7212935, 7239568, 7239570, 7239569, 7271873.

Product code FMF

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)