ARROW IPN047800Recalls & reported problems
Teleflex Incorporated · SnapLock(TM) Catheter/Syringe Adapter · Class 2
- 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 10801902137460), received between Mar 24, 2022 and Mar 24, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Disconnection” (1 report).
4 other recalls cover devices cleared under the same FDA submission (K103658); they may or may not involve this specific model.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Disconnection1
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.
MalfunctionMar 24, 2022Disconnection; Disconnection
WRITER NOTICED EPIDURAL CATHETER WAS DISCONNECTED WHILE REPOSITIONING PATIENT FROM SIDE TO SIDE. PATIENT'S DERMATOME LEVELS WERE T5. PART OF THE CATHETER THAT IS CONNECTED TO PATIENT WRITER LOCKED WITH STERILE SYRINGE. TAPE WAS INTACT OVER PATIENT'S BACK, NO MIGRATION OF CATHETER. DR. INSERTED NEW EPIDURAL CATHETER AND PATIENT WAS COMFORTABLE IN A FEW MINUTES AFTER INSERTION, FETAL HEART RATE AND BASELINE WAS THE SAME, NORMAL TRACING. MAYBE MANUFACTURER SHOULD SUGGEST PLACING TAPE OVER IT AND ALSO WHAT KIND OF TAPE SHOULD BE APPLIED. THERE IS NO WARNING (OR SUGGESTIONS FROM MANUFACTURER) ON THE PACKAGE THAT WE NEED TO USE TAPE OVER THESE PARTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13894305 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K103658. One submission often covers many models, so check the product and lot details in each record.
- Z-2364-2026 · Apr 21, 2026 · Open, ClassifiedDescription/REF: ACCESS TRAY/ASK-04001-SUH-S; ACCESS TRAY/ASK-04001-VM1; STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS; STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS;
- Z-1179-2020 · Jan 15, 2020 · TerminatedFlexTip Plus Epidural Catheterization Kit, Product Code ASK-05400-CA1
- Z-1962-2018 · Apr 11, 2018 · TerminatedSnapLock" Catheter/Syringe Adapter; Product Code: AS-05500
- Z-2462-2015 · Jul 30, 2015 · TerminatedPICC Kits with Peel-Away Sheath Component; catheter, intravascular, therapeutic, ultrasound Product Usage: catheter, intravascular, therapeutic, ultrasound
Other Anesthesia conduction kit devices
- BD Luer-Lok, BD Glaspak 405671Becton, Dickinson And Company · Anesthesia conduction kit1 recall68 reports
- ARROW IPN922678Teleflex Incorporated · Anesthesia conduction kit2 recalls0 reports
- BD Luer-Lok, BD Glaspak 405672Becton, Dickinson And Company · Anesthesia conduction kit1 recall27 reports
- BD Luer-Lok, BD Glaspak 405673Becton, Dickinson And Company · Anesthesia conduction kit1 recall10 reports
- BD Luer-Lok, BD Glaspak 405637Becton, Dickinson And Company · Anesthesia conduction kit1 recall7 reports
- BD Luer-Lok, BD Glaspak 405707Becton, Dickinson And Company · Anesthesia conduction kit1 recall4 reports
- BD Luer-Lok, BD Glaspak 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405735Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.