Search U.S. Product Recalls Database

Showing 7741–7760 of 11714 results

Sort:

MultiLab Series II REVO (Unetixs) – Air Embolism Risk (2023)

The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.

Moderate

FDAFeb 10, 2023Nationwide• Unetixs Vascular, Inc.

MultiLab Series II ROODRA (Unetixs) – Air Embolism Risk (2023)

The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.

Moderate

FDAFeb 10, 2023Nationwide• Unetixs Vascular, Inc.

Stay Informed

Search Product Recalls

MultiLab Series II REVO (Unetixs) – Air Embolism Risk (2023)

MultiLab Series II ROODRA (Unetixs) – Air Embolism Risk (2023)

Shiley Tracheal Tube (Covidien) – Inflation System Leak (2023)

MultiLab Series II LHS (Unetixs) – Air Embolism Risk (2023)

MultiLab Series II 2CP (Unetixs) – Air Embolism Risk (2023)

da Vinci Surgical System (Intuitive) – Manipulator Component Issue (2023)

DreamStation CPAP (Philips) – Communication Problem (2023)

DeRoyal Suction Canister (DeRoyal) – Lid Shrinkage Concern (2023)

Medtronic Grafton Gel (Medtronic) – Packaging Concern (2023)

Medtronic Grafton Orthoblend (Medtronic) – Packaging Concern (2023)

Medtronic Grafton DBF Inject (Medtronic) – Packaging Concern (2023)

Medtronic Grafton Crunch (Medtronic) – Packaging Concern (2023)

Medtronic Accelerate Grafton DBF (Medtronic) – Packaging Concern (2023)

Medtronic XPANSE Bone Insert (Medtronic) – Packaging Concern (2023)

Medtronic Grafton Putty (Medtronic) – Packaging Concern (2023)

Medtronic Grafton Matrix (Medtronic) – Packaging Concern (2023)

Medtronic Grafton Matrix Strips (Medtronic) – Packaging Concern (2023)

Medtronic Grafton Plus Paste (Medtronic) – Packaging Concern (2023)

Medtronic Grafton DBF (Medtronic) – Packaging Concern (2023)

Fentanyl and Ropivacaine Solution (Apollo Care) - Sterility Concern (2023)