Z-1525-06

BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950

Name: Z-1525-06 BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950
Creator: Becton Dickinson & Company
Published: 2006-07-24
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2006-07-24 / Terminated

FDA source

Becton Dickinson & Company began a recall of BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950 on 2006-07-24. The reason FDA records is "BD received reports of needle assembly disengagement from the syringe". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1525-06
Status: Terminated
Initiated: 2006-07-24
Posted: 2006-09-28
Terminated: 2007-12-03
Recalling firm: Becton Dickinson & Co
Product: BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950.
Product code: MEG Syringe, Antistick
Reason for recall: BD received reports of needle assembly disengagement from the syringe.
FDA root cause: Other
Action: Recall letters were sent to all wholesalers and end users on 7/28/2006.
Quantity in commerce: 1,294,200 units
Distribution: Nationwide.
Product codes and lots: Reorder Number: 305945 Lot: 5312395 and 5312394. Reorder Number: 305950 Lot: 5319508 and 5300175.

Product code MEG

K992734Class IIBecton Dickinson SyringeBd Becton Dickinson Vacutainer Systems Preanalytic / cleared 1999-10-01

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)