Civic Data
FDA RecallsUSDA RecallsAbout

FDA Recalls

  • Food recalls
  • Drug recalls
  • Device recalls

USDA Recalls

  • All USDA recalls
  • Poultry recalls
  • Meat recalls
  • Egg recalls

About

  • About us
  • FDA guides
  • USDA guides
  • Data sources
  • Privacy policy

Data

  • OpenFDA API
  • USDA FSIS

© 2026Civic Data · Data sourced from OpenFDA and USDA FSIS · Not affiliated with the U.S. Food and Drug Administration or the U.S. Department of Agriculture · Always verify against official sources before acting

  1. FDA Recalls
  2. ›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 881–900 of 1,000 recalls

Class IIOngoing

Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500

GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

May 1, 2026 · DeviceView details →
Class IIOngoing

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

Philips North America Llc

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

May 1, 2026 · Device
View details →
Class IIOngoing

CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040

INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

May 1, 2026 · DeviceView details →
Class IIOngoing

Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940

INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

May 1, 2026 · DeviceView details →
Class IIOngoing

Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models

GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

May 1, 2026 · DeviceView details →
Class IIOngoing

Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant warmer, Model Numbers 2082844-001-XXX

GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

May 1, 2026 · DeviceView details →
Class IIOngoing

CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030

INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

May 1, 2026 · DeviceView details →
Class IIOngoing

Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320

Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

April 30, 2026 · DeviceView details →
Class IIOngoing

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No

Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

April 30, 2026 · DeviceView details →
Class IIOngoing

Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320

Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

April 30, 2026 · DeviceView details →
Class IIOngoing

Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

April 30, 2026 · DeviceView details →
Class IIOngoing

BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neurovascular systems.

MICROVENTION INC.

Due to an increase rate of balloon pinhole defects.

April 30, 2026 · DeviceView details →
Class IIOngoing

Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

April 30, 2026 · DeviceView details →
Class IIOngoing

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20

Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

April 30, 2026 · DeviceView details →
Class IIOngoing

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24

Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

April 30, 2026 · DeviceView details →
Class IIOngoing

BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet

CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

April 30, 2026 · DeviceView details →
Class IIOngoing

Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320

Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

April 30, 2026 · DeviceView details →
Class IIOngoing

BD Pyxis Mini Main REF: 349 Medication cabinet

CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

April 30, 2026 · DeviceView details →
Class IIOngoing

Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

April 30, 2026 · DeviceView details →
Class IIOngoing

Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

April 30, 2026 · DeviceView details →
← PreviousPage 45 of 50Next →