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Safety Reports: Medical Devices

Updated:

Spectrum IQ Infusion Pumps - recalled due to Multiple Connectivity Errors, USA

2 years ago •source fda.gov • details

Recall notice

Company name: Baxter International Inc.
Brand name: Spectrum IQ
Product recalled: Infusion Pumps
Reason of the recall: Multiple Connectivity Errors
FDA Recall date: August 24, 2021
Recall details: Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for all Spectrum IQ infusion pumps… See more

#recall #medicaldevices #us

321

Monoject Flush Prefilled Saline Syringes - recalled due to air reintroducing into the syringe, USA

2 years ago •source fda.gov • details

Recall notice

Company name: Cardinal Health
Brand name: Monoject
Product recalled: Flush Prefilled Saline Syringes
Reason of the recall: Products have been found to reintroduce air into the syringe after the air has been expelled
FDA Recall date: August 20, 2021
Recall details: On August 4, 2021, Cardinal Health… See more

#blood #recall #medicaldevices #us

Monoject Flush Prefilled Saline Syringes - recalled due to air reintroducing into the syringe photo #1
321

Ultrasound Gel - recalled due to product is contaminated with bacteria, USA

2 years ago •source fda.gov • details

Recall notice

Company name: Eco-Med Pharmaceutical
Brand name: Multiple brand names
Product recalled: Ultrasound Gel
Reason of the recall: Product is contaminated with bacteria (Burkholderia cepacia complex)
FDA Recall date: August 04, 2021
Recall details: Etobicoke, Ontario (August 4, 2021) – Eco-Med Pharmaceuticals, Inc. today commenced a voluntary recall… See more

#recall #medicaldevices #us

321

BD Alaris System - recalled due to Infusion pump may not operate as expected, USA

2 years ago •source fda.gov • details

Recall notice

Company name: Becton, Dickinson and Company
Brand name: BD
Product recalled: Alaris System
Reason of the recall: Infusion pump may not operate as expected
FDA Recall date: August 02, 2021
Recall details: FRANKLIN LAKES, N.J., July 29, 2021 /PRNewswire/ BD (Becton, Dickinson and Company) (NYSE: BDX), a… See more

#blood #recall #medicaldevices #us

321

Hypodermic Needle Insulin Syringes - recalled due to skewed markings on syringes, USA

3 years ago •source fda.gov • details

Recall notice

Company name: Smiths Medical
Brand name: Jelco
Product recalled: Hypodermic Needle-Pro Fixed Needle Insulin Syringes
Reason of the recall: Skewed odd number line graduation markings on syringe barrels.
FDA Recall date: June 17, 2021
Recall details: Company Announcement Smiths Medical has become aware of specific models and… See more

#recall #medicaldevices #us

321

Philips pressure and mechanical ventilator devices - recalled due to health risks, USA

3 years ago •source fda.gov • details

Recall notice

Company name: Philips
Brand name: Philips
Product recalled: Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices
Reason of the recall: Potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam component in these devices
FDA Recall date:… See more

#recall #medicaldevices #us

321

ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator - recalled due to defective applicator, USA

3 years ago •source fda.gov • details

Recall notice

Company name: Becton, Dickinson and Company
Brand name: ChloraPrep
Product recalled: ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator
Reason of the recall: Defective applicator
FDA Recall date: April 20, 2021
Recall details: BD (Becton, Dickinson and Company), a leading global medical technology company, is voluntarily recalling specified lots… See more

#blood #medicaldevices #recall #us #orange

321

Tenacore LLC 2001 Tenacore Replacement CareFusion Alaris 8100 bezels - recalled due to Potentially weakened elastic, USA

3 years ago •source fda.gov • details

Recall notice

Company name: Tenacore LLC
Brand name: Tenacore LLC
Product recalled: 2001 Tenacore Replacement CareFusion Alaris 8100 bezels
Reason of the recall: Potentially weakened elastic
FDA Recall date: April 19, 2021
Recall details: Company Announcement On February 24th, 2021, Tenacore LLC initiated a nationwide recall of 2001 Tenacore… See more

#medicaldevices #us

Tenacore LLC 2001 Tenacore Replacement CareFusion Alaris 8100 bezels - recalled due to Potentially weakened elastic photo #1
322

Medtronic Valiant Navion™ Thoracic stent graft system - recalled due to endoleaks, stent fractures and stent ring enlargement, USA

3 years ago •source fda.gov • details

Recall notice

Company name: Medtronic
Brand name: Medtronic Valiant Navion™
Product recalled: Thoracic stent graft system
Reason of the recall: Due to endoleaks, stent fractures and stent ring enlargement
FDA Recall date: February 23, 2021
Recall details: Medtronic plc (NYSE:MDT), the global leader in medical technology, has voluntarily issued… See more

#recall #medicaldevices #us

321

Wahl Clipper Deluxe Heat Therapy Massagers - recalled due to fire hazard, USA

3 years ago •source fda.gov • details

Recall notice

Company name: Wahl Clipper Corporation
Brand name: Wahl
Product recalled: Deluxe Heat Therapy Massagers, Model 4212
Reason of the recall: Can overheat causing smoke or spark, which may pose a fire hazard
FDA Recall date: January 28, 2021
Recall details: Wahl Clipper Corporation is voluntarily recalling all… See more

#medicaldevices #us

Wahl Clipper Deluxe Heat Therapy Massagers - recalled due to fire hazard photo #1
321

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