FDA Device Intelligence
Home › Device types › PND

Midline Catheter

FDA product code PND · Class 2 · General Hospital

279
Registered devices
983
Adverse events
10
Recalls
13
510(k) clearances

Devices with this code

Midline Catheter Kit — Bard Access Systems, Inc.PowerMidline — Bard Access Systems, Inc.PowerMidline — Bard Access Systems, Inc.PowerMidline — Bard Access Systems, Inc.SURFLO MIDELA — Terumo Medical Products (Hangzhou) Co., Ltd.Midline Catheter Kit — Bard Access Systems, Inc.ARROW — TELEFLEX INCORPORATEDSURFLO MIDELA — Terumo Medical Products (Hangzhou) Co., Ltd.PowerMidline — Bard Access Systems, Inc.SURFLO MIDELA — Terumo Medical Products (Hangzhou) Co., Ltd.primeMIDLINE — PFM MEDICAL INCORPORATEDPowerMidline — Bard Access Systems, Inc.Provena Midline — Bard Access Systems, Inc.VYGON — Vygon CorporationPeripheral Catheter Insertion Kit — Bard Access Systems, Inc.SURFLO MIDELA — Terumo Medical Products (Hangzhou) Co., Ltd.Midline Catheter Kit — Bard Access Systems, Inc.Peripheral Catheter Insertion Kit — Bard Access Systems, Inc.Midline Catheter Kit — Bard Access Systems, Inc.BioFlo — NAVILYST MEDICAL, INC.ARROW — TELEFLEX INCORPORATEDPowerMidline — Bard Access Systems, Inc.Provena Midline — Bard Access Systems, Inc.VYGON — Vygon Corporation

Recent recalls

DateFirmReason
2026-05-21Bard Access Systems, Inc.Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie
2026-05-21Bard Access Systems, Inc.Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie
2026-05-21Bard Access Systems, Inc.Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie
2026-04-21ARROW INTERNATIONAL, LLCLidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss
2022-09-14ARROW INTERNATIONAL Inc.Mislabeling: the corrugate label, lidstock, banner card, and peel sticker accompanying the affected product incorrectly displays a double lumen 5.5 French cath
2020-09-14Becton Dickinson & CompanyKits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.
2020-09-14Becton Dickinson & CompanyKits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.
2020-03-17Becton Dickinson & CompanyIincorrectly packaged without the required lidocaine as labeled
2019-09-24Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT Midline Basic Tray.
2019-04-23Arrow International IncLidstock states the incorrect expiration date for the product

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.