ClearanceBrief
510(k) K980987 ยท FMF Syringe, Piston

BECTON DICKINSON SYRINGE

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US
DecisionSubstantially Equivalent, Jun 11, 1998
ReceivedMar 17, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980987

DateFirm and productCodeLinked 510(k)
Mar 6, 2026Becton Dickinson & Company
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Open, Classified
FMFNone listed
Dec 23, 2020Becton Dickinson & Company
BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
Terminated
FMFNone listed
Feb 1, 2019Becton Dickinson & Company
3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
Terminated
FMFNone listed
Dec 19, 2012Becton Dickinson & Company
Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD, Franklin Lakes, NJ 07417 USA Made in USA www.bd.com BD, Laagstraat 57, B-9140 Temse, Belgium On 100 unit plastic bag: BD oral sy
Terminated
FMFNone listed
May 24, 2007Becton Dickinson & Company
BD 5ml Syringe Luer-Lok Tip Bulk Sterile Convenience Pak Latex Free
Terminated
FMFNone listed
Apr 5, 2007Becton Dickinson & Company
BD 30ml Syringe Luer-Lok tip Sterile BD, Franklin Lakes, NJ Made in USA
Terminated
FMFNone listed
Jul 28, 2005Becton Dickinson & Company
# 309603 -- Syringe 5Ml LL syringe.
Terminated
FMFNone listed
Jul 28, 2005Becton Dickinson & Company
# 309604 -- Syringe 10 mL LL
Terminated
FMFNone listed
Jul 28, 2005Becton Dickinson & Company
#309661 -- Syringe only ll 20 mL
Terminated
FMFNone listed
Jul 28, 2005Becton Dickinson & Company
#309644 -- 10 ml syringe with 20 G1'' Needle
Terminated
FMFNone listed
Jul 28, 2005Becton Dickinson & Company
#309604 -- 10 mL syringe
Terminated
FMFNone listed
Sep 11, 2003Bard Endoscopic Technologies
Bard PEG Safety System ''Guidewire'' Reorder Number: 000930
Terminated
FMFNone listed
Sep 11, 2003Bard Endoscopic Technologies
Bard Ponsky PEG Safety System ''Pull'' Reorder Number: 001925
Terminated
FMFNone listed
Sep 11, 2003Bard Endoscopic Technologies
Bard Ponsky PEG Safety System ''Pull'' Reoder Number: 001927
Terminated
FMFNone listed
Sep 11, 2003Bard Endoscopic Technologies
Bard PEG Safety System ''Guidewire'' Reorder Number: 001928
Terminated
FMFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.