BD IV Start Pak, BD Persist 386172Recalls & reported problems

Becton, Dickinson And Company · IVSS RED IV ACC WO TEGADERM MED GLVS · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30382903861720), received between Sep 22, 2024 and Sep 22, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Device Markings/Labelling Problem1

Patient problems

No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

MalfunctionSep 22, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT BD IVSS BLUE IV ACC WO TEGADERM MED GLVS EXPIRED PRODUCT RECEIVED 357.13BX ( (B)(4) EA ) EXPIRED WITH GUARANTEE LETTER. THIS REPORT IS EXPIRED PRODUCT WITH GUARANTEE LETTER ISSUED BY BECTON DICKINSON, THERE ARE 3 LOT NUMBERS WITH THE SAME ARTICLE. THE FOLLOWING ARE THE EXPIRED ITEM WITH CORRESPONDING LOT NUMBER AND QUANTITY : 2278835- (B)(4) EA, 2278838-28,(B)(4) EA, 2278840- (B)(4) EA.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20276042 ↗

Device details

UDI-DI	`30382903861720`
Brand	BD IV Start Pak, BD Persist
Model	386172
Company	Becton, Dickinson And Company
Product code	LRS · I.V. start kit
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Dec 11, 2019

Device type (GMDN): Peripheral intravenous catheterization support kit

A collection of noninvasive devices intended to prepare and/or dress a peripheral vein intravenous (IV) access site. It typically includes devices such as a tourniquet, disinfected swabs, dressings, tape, gauze, and gloves; neither the IV access device nor pharmaceuticals are included. It may also include short tubing and/or syringe, however it is not intended to directly conduct fluids from an IV administration bag/bottle (i.e., not an IV administration set). This is a single-use device.

Other I.V. start kit devices

Medline Industries, Inc. CDS860014P
Medline Industries, Inc. · I.V. start kit
3 recalls0 reports
Medline Industries, Inc. DYKM1000B
Medline Industries, Inc. · I.V. start kit
3 recalls0 reports
MEDLINE DYNJ68937A
Medline Industries, Inc. · I.V. start kit
2 recalls2 reports
Centurion IVS3940B
Centurion Medical Products Corporation · I.V. start kit
2 recalls0 reports
Centurion CVI3650
Centurion Medical Products Corporation · I.V. start kit
2 recalls0 reports
MEDLINE DYNDV2465
Medline Industries, Inc. · I.V. start kit
2 recalls0 reports
MEDLINE PICC0010
Medline Industries, Inc. · I.V. start kit
2 recalls0 reports
Centurion IVS3900A
Centurion Medical Products Corporation · I.V. start kit
2 recalls0 reports

All I.V. start kit devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

How reports and recalls are matched · Editorial policy · Report an error on this page