Z-0402-06

BD 1 mL BD Safety Glide tuberculin syringe with 27 G x 1/2 in. BD needle

Name: Z-0402-06 BD 1 mL BD Safety Glide tuberculin syringe with 27 G x 1/2 in. BD needle
Creator: Becton Dickinson & Company
Published: 2005-10-25
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2005-10-25 / Terminated

FDA source

Becton Dickinson & Company began a recall of BD 1 mL BD Safety Glide tuberculin syringe with 27 G x 1/2 in. BD needle on 2005-10-25. The reason FDA records is "Safety mechanisms on the syringes are rotating too freely. This can result in the safety mechanism not holding its rotational position and increasing risk of an accidental needle-stick". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0402-06
Status: Terminated
Initiated: 2005-10-25
Posted: 2006-01-18
Terminated: 2006-06-21
Recalling firm: Becton Dickinson & Co
Product: BD 1 mL BD Safety Glide tuberculin syringe with 27 G x 1/2 in. BD needle.
Product code: FMF Syringe, Piston
Reason for recall: Safety mechanisms on the syringes are rotating too freely. This can result in the safety mechanism not holding its rotational position and increasing risk of an accidental needle-stick.
FDA root cause: Other
Action: Recall notifications were sent to all direct consignees and potential end users on 10/25/2005 via UPS second day air.
Quantity in commerce: 6920 cases -- 2768000 syringes
Distribution: Product was distributed nationwide to 450 consignees composed of wholesalers, hospitals, and medical supply distributors. There is a Canadian customer, Dufort & Lavigne, Montreal, Quebec, Canada. Government customers include VAMC New Orleans, New Orleans, LA; Fox Army Health Center, Redstone Arsenal, AL; Moncrief Army Community Hospital, Columbia, SC; US Naval Med. Ctr., Portsmouth, VA; USAF Hill AFB 649 Medical Group, Hill Air Force Base, UT; VAMC Ann Arbor, MI; VAMC East Orange, NJ; VAMC Tuskegee, AL; McDonald Army Community Hospital, Newport News, VA.
Product codes and lots: Reference Number 305945: 1mL 27G Blister: Lot #: 5201851; 5201855; 5201853; 5175734; 5175732; 5175731; 5175730; 5146694; 5146689; 5146686; 5146691; 5146688; 5115764; 5111314; 5111313; 5082345; 5082341; 5082350; 5082344; 5052275; 5052276; 4344969; 4344970; 4344930; 4344978; 4344934; 4323196; 4323195; 4323194; 4296986.

Product code FMF

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)