Z-0582-2007

BD Integra 1ml Insulin Syringe with Retracting Precision Guide Needle 1 ml 29g 1/2'' (0.33mm x 13 mm)...

Name: Z-0582-2007 BD Integra 1ml Insulin Syringe with Retracting Precision Guide Needle 1 ml 29g 1/2'' (0.33mm x 13 mm)...
Creator: Becton Dickinson & Company
Published: 2007-01-27
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2007-01-27 / Terminated

FDA source

Becton Dickinson & Company began a recall of BD Integra 1ml Insulin Syringe with Retracting Precision Guide Needle 1 ml 29g 1/2'' (0.33mm x 13 mm) Re-Order No. 305282 U-100 insulin Lot 6073436 on 2007-01-27. The reason FDA records is "The needle becomes detached from the hub/syringe". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0582-2007
Status: Terminated
Initiated: 2007-01-27
Posted: 2007-03-03
Terminated: 2007-07-24
Recalling firm: Becton Dickinson & Co
Product: BD Integra 1ml Insulin Syringe with Retracting Precision Guide Needle 1 ml 29g 1/2'' (0.33mm x 13 mm) Re-Order No. 305282 U-100 insulin Lot 6073436
Product code: FMF Syringe, Piston
Reason for recall: The needle becomes detached from the hub/syringe
FDA root cause: Other
Action: Recall notification letters were sent via UPS second day air on January 27, 2007. Distributors were asked to provide end user contact information to recalling firm.
Quantity in commerce: 247,824 units
Distribution: Nationwide
Product codes and lots: Lot # 6073436 Ref (Reorder number) 305282)

Product code FMF

K023752Class IIBd Integra SyringeBd / cleared 2003-02-07

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)