Every recall we track for Covidien — 18 in all — plus the complaints and injury reports the public filed about them.
Covidien recalls bedside SpO2 monitors that may not alert users to low oxygen levels, risking respiratory failure. Check if your monitor has model numbers listed in the recall notice.
Covidien is a leading manufacturer of medical devices and surgical products, including endoscopic and surgical instruments, wound care products, and more.
Covidien recalls Shiley Adult Flexible Tracheostomy Tubes with TaperGuard Cuff Reusable Inner Cannula due to potential disconnection causing respiratory failure or death.
Covidien is a leading manufacturer of medical devices, including surgical instruments, endoscopic equipment, and more.
Covidien is a leading manufacturer of medical devices and surgical products, including endoscopic and surgical instruments, catheters, and more.
Covidien is a leading manufacturer of medical devices, including surgical instruments, endoscopic equipment, and more.
Puritan Bennett 560 ventilators used for more than 14 years of cumulative service may release harmful VOCs. Owners should check if their device was sold before June 2024 with specific serial numbers.
Covidien recalls specific laparotomy sponges that may not be properly sterilized, risking infection and tissue damage during surgery. Affected sponges have unique identifiers and were sold in certain lots.
Covidien recalls Medtronic Invos reusable sensor cables for PM7100 devices with manufacturing defects that may cause error codes or non-functioning channels. Affected units have specific lot numbers and UDI codes.
Covidien recalls reusable infant sensor adapter cables for Medtronic Invos PM7100 monitors due to manufacturing defects causing error codes or non-functioning channels. Affected units have specific lot numbers and UDI codes.
Covidien recalls Valleylab FT10 Energy Platform systems with software v4.0.1-4.0.3 that may become inoperable due to a software error. Affected units include specific model references and serial numbers.
Covidien recalls stolen McGRATH MAC Video Laryngoscopes (REF: 301-000-000) that failed quality tests. Defective units may cause failed laryngoscopy or intubation during medical procedures.
Puritan Bennett recalls 180-03 Cuff Pressure Manager units with serial numbers E223500003-E225000099. Inadequate internal fixation of the power port may cause detachment after use, preventing charging and risking treatment delays.
Covidien recalls McGrath Mac 2 disposable laryngoscope blades (REF 350-084-000) due to potential condensation causing blurred vision during use. Affected items have specific UDI and lot numbers.
Covidien recalls McGrath Mac 2 disposable laryngoscope blades with possible condensation causing blurred screens. Affected items have specific UDI and lot numbers.
Shiley recalls adult flexible tracheostomy tubes with TaperGuard Cuff and cuffless models due to a manufacturing error causing smaller than specified connectors, which can lead to respiratory failure or bleeding if not securely connected.
Covidien recalls Shiley Lo-Pro Oral/Nasal Tracheal Tubes with potential leaks in the cuffed inflation system. Affected units include model REF 86051, 7.0 mm I.D. with specific lot numbers. Contact for replacement or return.
Covidien recalls Surgiwand II suction devices due to particulate matter in tubing from damaged Y-connector during assembly. Affected models include 178083, 178093, 178094.
