Covidien recalls
Every recall we track for Covidien — 18 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them. 5 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Covidien fell by more than half in 2025 (3, down from 7 in 2024). 28% rated “stop using now”.
All FDA recall records for Covidien since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 2 | 2 | 3 | 0 | 7 |
| 2024 | 1 | 0 | 6 | 0 | 7 |
| 2025 | 2 | 1 | 0 | 0 | 3 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Covidien product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Covidien recalls
15 shown- Use cautionMedical device
Covidien recalls Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,
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.
CovidienJun 23, 2025 - Stop using nowMedical device
Covidien recalls Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,
Covidien recalls Newport HT70 Ventilators with specific model numbers due to potential failure of printed circuit board assembly causing shutdowns or alarm failures, which could lead to respiratory issues.
CovidienMay 21, 2025 - Stop using nowMedical device
Covidien recalls Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula, REF: 7CN80R
Covidien recalls Shiley Adult Flexible Tracheostomy Tubes with TaperGuard Cuff Reusable Inner Cannula due to potential disconnection causing respiratory failure or death.
CovidienFeb 26, 2025 - Lower riskMedical device
Covidien recalls Covideien McGRATH MAC Video Laryngoscope, REF: 301-000-000, Non-Sterile, RxOnly
Covidien is a leading manufacturer of medical devices and surgical products, including endoscopic and surgical instruments, catheters, and more.
CovidienJul 9, 2024 - Lower riskMedical device
Covidien recalls McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only
Covidien is a leading manufacturer of medical devices, including surgical instruments, endoscopic equipment, and more.
CovidienJul 9, 2024 - Lower riskMedical device
Covidien recalls Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560
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.
Puritan BennettJun 24, 2024 - Stop using nowMedical device
Covidien recalls Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1
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.
CovidienFeb 21, 2024 - Lower riskMedical device
Covidien recalls Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC
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.
CovidienJan 9, 2024 - Lower riskMedical device
Covidien recalls Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD
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.
CovidienNov 16, 2023 - Stop using nowMedical device
Covidien recalls Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
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.
CovidienSep 28, 2023 - Use cautionMedical device
Covidien recalls Puritan Bennett Cuff Pressure Manager, REF: 180-03
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.
Puritan BennettAug 22, 2023 - Lower riskMedical device
Covidien recalls McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Covidien recalls McGrath Mac 2 disposable laryngoscope blades with possible condensation causing blurred screens. Affected items have specific UDI and lot numbers.
CovidienAug 10, 2023 - Use cautionMedical device
Covidien recalls Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner
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.
ShileyMar 24, 2023 - Stop using nowMedical device
Covidien recalls COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube
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.
CovidienFeb 10, 2023 - Lower riskMedical device
Covidien recalls Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product
Covidien recalls Surgiwand II suction devices due to particulate matter in tubing from damaged Y-connector during assembly. Affected models include 178083, 178093, 178094.
CovidienMar 5, 2021
Covidien recall questions
How many recalls has Covidien had?
18 recalls from Covidien are on record with U.S. safety agencies, from 2021–2025.
What is the most recent Covidien recall?
Covidien recalls Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,, dated Jun 23, 2025. Every Covidien recall is listed on this page, newest first.
What should I do if I have a recalled Covidien product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Covidien recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.