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Displaying 1 - 7 of 7 items.
Sofsilk™ Braided Silk sutures and Ti-Cron™ Coated Braided Polyester Sutures
Specific lots of the Sofsilk™ Braided Silk sutures and Ti-Cron™ Coated Braided Polyester Sutures were sterilized with gamma doses that exceeded the range approved or were exposed to more than the approved number of Ethylene Oxide (EO) sterilization…
RecallHealth product recall | 2024-01-31
Mahurkar Acute High Pressure Triple Lumen Catheter Kit Curved Extensions
During manufacturing related testing, the catheter center lumen was found to have an occlusion in the tip of the catheter. The source of the occlusion is excessive mdx, a silicone-based lubricant which coats the catheter tip.
Recall Start Date: June…
RecallHealth product recall | 2023-07-07
Surgical Gut - Plain and Absorbable Sutures
Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product.
Recall start date: March 1, 2023
RecallHealth product recall | 2023-03-17
Tri-Staple™ 2.0 Black Intelligent Reload
Specific lots have the potential for a broken sled vane component. A broken sled vane may cause the reload to misfire leading to non-functional staple line closure, transecting tissue without forming staples, and tissue hang-up. These conditions may…
RecallHealth product recall | 2023-02-08
Medtronic Nonabsorbable Sutures
Medtronic has determined that there were manufacturing errors in the packaging of the listed nonabsorbable sutures that may cause a gap or wrinkle in the breather pouch seal resulting in a sterile barrier breach. The potential harms of a sterile barrier…
RecallHealth product recall | 2022-12-13
Puritan Bennett 560 Ventilator
Medtronic is issuing a voluntary medical device correction related to specific serial numbers of the turbine component of Puritan Bennett 500 series ventilators. This voluntary medical device correction is being issued following confirmation of six…
RecallHealth product recall | 2022-08-31
Puritan Bennett 980 Series Ventilator
This voluntary medical device correction is being taken following the investigation of six customer reports stating that a total of four ventilators became inoperable during use. One of these reports indicated that, following the ventilator becoming…
RecallHealth product recall | 2021-11-29