All Recalls

95,083 total recalls in our database

Sagittal MICRO-SAW

The Anspach Effort

🏥 Medical Devices Class I - Dangerous

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Oct 6, 2016 Other Medical Devices Nationwide View Details →

Pediatric Craniotome

The Anspach Effort

🏥 Medical Devices Class I - Dangerous

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Oct 6, 2016 Other Medical Devices Nationwide View Details →

14cm QD Angle Attachment

The Anspach Effort

🏥 Medical Devices Class I - Dangerous

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Oct 6, 2016 Other Medical Devices Nationwide View Details →

They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.

Mar 30, 2017 Implants & Prosthetics Nationwide View Details →

ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.

Mar 24, 2017 Infusion Pumps Nationwide View Details →

Medtronic is issuing a voluntary field corrective action for all its Newport" HT70 and Newport" HT70 Plus ventilators because they may shutdown spontaneously during normal operation without an accompanying alarm.

Mar 30, 2017 Patient Monitors Nationwide View Details →

Chuck Driver System

The Anspach Effort

🏥 Medical Devices Class I - Dangerous

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Oct 6, 2016 Infusion Pumps Nationwide View Details →