RecallRadar

FDA Device recall Z-2055-2018

BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983

On 2018-06-13 the FDA classified a Class II recall of BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983 by Becton Dickinson And, citing tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2055-2018
ClassificationClass II
Statusterminated
Initiated2018-02-13
Published2018-06-13
Last updated2026-09-13 11:54 UTC
CompanyBecton Dickinson And
DistributionUS

Product

BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983

Reason

Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube

Identifiers

code_info
1) UDI DI (01)50382903679831 PI (17)180531(10)7135828(30)1000 Lot/Serial # 7315828 Exp Date 5/31/2018 2) UDI DI (…1) UDI DI (01)50382903679831 PI (17)180531(10)7135828(30)1000 Lot/Serial # 7315828 Exp Date 5/31/2018 2) UDI DI (01)50382903679831 PI (17)180531(10)7146901(30)1000 Lot/Serial # 7125692 Exp Date 4/30/2018

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2055-2018%22

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