PlainRecalls

Covidien

21 recalls on record · Latest: Jul 30, 2025

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Agency notice ledger

Federal filing book Covidien MID-BOOK · SINGLE-AGENCY

#765 of 14,151 · 21 notices · 0.020% archive

  • BOOK 21 notices
  • RANK #765 of 14,151
  • SHARE 0.020% archive
  • AGENCY FDA Devices (21)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 30, 2025
  • PHOTO A&h Focal Inc.

Nearest notice-volume peer: A&h Focal Inc. (0 notice gap)

Covidien accounts for about 0.020% of the 104,423-notice archive on 21 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Covidien sits among 14,151 recalling firms

Covidien ranks 765th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Covidien vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

21 765th of 14151 higher than 13,362 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-10-31

Covidien in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Covidien holds about 0.020% of archive notices alongside 21 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026
FDA Devices Moderate Jul 30, 2025

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J, 10005941JP, 10005941JPN

FDA Devices Critical Jun 18, 2025

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU, HT70M-WW-NA, HT70-SY-EU. Newport HT70Plus Ventilator, REF: HT70PM-ES-EU, HT70PM-ES-NA, HT70PM-JP-NA, HT70PM-PT-BR, HT70PM-SY-AS, DLHT70PM-WW-NA, HT70PM-SY-NA, HT70PM-SY-UK, HT70PM-WW-EU, HT70PM-WW-UK, HT70PM-SY-EU, HT70PM-WWNA. HT70-2 CONTROL BOARD ROHS X1, REF: GR105796. HT70P CONTROL BOARD ROHS X1, REF: GR105795. HT70 Conversion Kit, REF: GRFSKHT70M-2.

FDA Devices Critical Apr 2, 2025

Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula, REF: 7CN80R

FDA Devices Critical Aug 28, 2024

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

FDA Devices Moderate Aug 28, 2024

Covideien McGRATH MAC Video Laryngoscope, REF: 301-000-000, Non-Sterile, RxOnly

FDA Devices Critical Aug 28, 2024

McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , Non-Sterile, Rx Only

FDA Devices Critical Aug 14, 2024

Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560 VENTILATOR EU-DIV/4096600-01, PURITAN BENNETT 560 VENTILATOR JAPAN/4096600-02, PURITAN BENNETT 560 VENTILATOR APAC/4096600-03, Puritan Bennett 560 Ventilator LATAM/4096600-04, Puritan Bennett 560 Ventilator EMEA/4096600-05, Puritan Bennett 560 Ventilator CAN ANZ/4096600-06, Puritan Bennett 540 Ventilator USA/4097100 Puritan Bennett 520 Ventilator/4098300, Puritan Benn

FDA Devices Moderate May 8, 2024

Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC

FDA Devices Moderate May 8, 2024

Medtronic Invos, Reusable Sensor Cable for PM7100, REF: PMAC71RSC

FDA Devices Moderate Mar 27, 2024

Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1

FDA Devices Moderate Jan 10, 2024

Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD

FDA Devices Moderate Nov 8, 2023

McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only

FDA Devices Moderate Nov 8, 2023

McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

FDA Devices Critical Nov 8, 2023

Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000

FDA Devices Moderate Oct 11, 2023

Puritan Bennett Cuff Pressure Manager, REF: 180-03

FDA Devices Critical Apr 26, 2023

Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner Cannula (REF, Product Description): 10CN10H, 10.0MM SHILEY CUFFED TRACH CAN; 10CN10R, 10.0MM ADT FLEX TRACH W TG CUFF; 10UN10A, 10.0MM UNCUFF TRACH TUBE X1; 10UN10H, 10.0MM SHILEY CUFFLESS TRACH C; 10UN10R, 10.0MM ADT FLEX TRACH CUFFLESS; 4CN65A, 6.5MM TRACH TUBE W TG CUFF X1; 4CN65H, 6.5MM SHILEY CUFFED TRACH CANN; 4CN65R, 6.5MM ADT FLEX TRACH W TG CUFF X1; 4UN65A, 6.

FDA Devices Moderate Apr 5, 2023

COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed are indicated for airway management by oral/nasal intubation of the trachea for anesthesia or other short-term procedures.

FDA Devices Moderate Apr 21, 2021

Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product Number/CFN: 178083, 178093, 178094

FDA Devices Critical Feb 11, 2015

Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025, CVT812015, and CVT812025. The following models are not offered for sale in the US: EVT808015, EVT808025, EVT812015, and EVT812025 Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

FDA Devices Critical Feb 11, 2015

Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

FDA Devices Critical Jan 15, 2014

Puritan Bennett 840 ventilator systems software part number 4-070212-85, revision AB-AG. The intended use of the product is to provide mechanical ventilation to patients.

Covidien holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (21 here).

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Frequently Asked Questions

How many federal recall notices name Covidien? ▼
PlainRecalls indexes 21 distinct federal recall events naming Covidien, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of October 2026). That count is an issuance inventory, not a hazard score.
Where does Covidien sit among other recalling firms? ▼
Covidien ranks #765 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Covidien's notices? ▼
FDA Devices accounts for 21 of this firm's 21 indexed notices.
What product category dominates Covidien's filing book? ▼
Filings for Covidien span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Covidien: 21 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Covidien; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of October 2026