PlainRecalls

Covidien LLC

Compiled from official public sources by the publisher.

340 recalls on record · Latest: Jul 8, 2026

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Agency notice ledger

Federal filing book Covidien LLC HEAVY-BOOK · SINGLE-AGENCY

#28 of 14,151 · 340 notices · 0.326% archive

  • BOOK 340 notices
  • RANK #28 of 14,151
  • SHARE 0.326% archive
  • AGENCY FDA Devices (340)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 8, 2026
  • PHOTO C & S Wholesale Groce…

Nearest notice-volume peer: C & S Wholesale Grocers Inc. (2 notice gap)

Covidien LLC accounts for about 0.326% of the 104,423-notice archive on 340 distinct filings — a heavy 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 LLC sits among 14,151 recalling firms

Covidien LLC ranks 28th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Covidien LLC vs all firms by recall-notice count

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

340 28th of 14151 higher than 14,123 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 · 2026-09-13

Covidien LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Covidien LLC holds about 0.326% of archive notices alongside 340 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 8, 2026

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the Covidien Shiley Disposable Decannulation Plug are: Product Number / UDI-DI code 4DCFN 10884522006576 4DCFS 10884522006583 4DFEN 10884522006606 6DCFN 10884522006613 6DCFS 10884522006620 6DFEN 10884522006644 8DCFN 10884522006651 8DCFS 40884522006690 8DFEN 10884522006675 10DCFN 20884522006535 10DCFS 10884522006545 10DFEN 10884522006569 The Shiley Disposable Decann
FDA Devices Moderate Jun 10, 2026

Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
FDA Devices Moderate Jun 10, 2026

COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028 The devices are intended for use in providing tracheal access for airway management. Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of polyvinyl chloride.
FDA Devices Moderate Jun 10, 2026

Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
FDA Devices Moderate Jun 10, 2026

Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
FDA Devices Moderate Mar 18, 2026

HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 10884521844940 Vital Sync 3.4.1 / 10884521847569 (OUS Only) Vital Sync 3.4.2 / 10884521856127 Product Number: VSLBASE04P / VITALSYNCSW04 Model / UDI-DI codes: Vital Sync 4.0.0 / 10884521849358 Vital Sync 4.0.2 / 10884521856134 The Vital Sync" Informatics Manager is software that is intend
FDA Devices Moderate Jun 19, 2024

EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx Only
FDA Devices Moderate Aug 9, 2023

Covidien Cytosponge Cell Collection Device, REF: CYTO-201; and Covidien Cytosponge Cell Collection Kit, REF: CYTO-KIT-USM
FDA Devices Moderate Jul 5, 2023

Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS
FDA Devices Moderate Jan 18, 2023

COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
FDA Devices Moderate Sep 28, 2022

Puritan Bennett 560 Ventilator, PB560, CFN 4096600
FDA Devices Moderate Aug 3, 2022

TruClear Hysteroscopic Tissue Removal System Control Unit- designed to meet the requirements of intrauterine tissue removal. Model Number: 7209808
FDA Devices Critical Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Palindrome Precision HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Palindrome H Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Palindrome SI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Mahurkar Chronic Carbothane (Maxid) Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Palindrome Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Palindrome Precision H Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Palindrome Precision SI Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Critical Jul 13, 2022

Palindrome HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
FDA Devices Moderate Feb 9, 2022

Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm, Chameleon PTA Balloon Catheter with Injection Port 8 mm x 40 mm; Cardiovascular. Product Numbers CH08-40-75GB and CH08-40-75US
FDA Devices Moderate Jan 19, 2022

LigaSure Blunt Tip Laparoscopic Sealer/Divider, Nano-Coated, Product Number LF1837
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X2ESDIEC
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980U1ESDIUC
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980U1ENASAA
FDA Devices Moderate Dec 15, 2021

Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information on the battery charging progress and battery pack status Item Code: CBCA
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X3ENDIUU
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X1ENNISB
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980S3ENDICU
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980A3ENNISB
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X1ENDIPC
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980S1ENDICU
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X1ENDIUU
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980A1ENNISB
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X1JADIJJ
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator,980X1ENAIQC
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980U3ESDIUU
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X3JADIJJ
FDA Devices Critical Dec 15, 2021

Puritan Bennett 980 Series Ventilator, 980X1PLDIPC
FDA Devices Moderate Nov 17, 2021

Covidien Emprint Ablation Catheter with Thermosphere Technology Bronchoscopic Ablation, CFN CA108L1
FDA Devices Moderate Aug 18, 2021

Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic energy to drive the active blade. Product Number: SCGAA
FDA Devices Moderate Apr 21, 2021

Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For use with Signia stapling system. Staple line reinforcement has applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection of tissue and creation of anastomosis. It may be used for transection and resection of liver substance, hepatic vasculature and biliary structures, and for transection and resection of pancreas. Product Number: SIGTRSB60AMT
FDA Devices Moderate Apr 7, 2021

CF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age.
FDA Devices Moderate Apr 7, 2021

BRAVO PH CAPS DELIVERY DEV5-PK, FGS-0312/FGS-0313 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age.
FDA Devices Moderate Mar 3, 2021

Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the repair of inguinal hernias via laparoscopic or posterior open procedures Item Code: TECT1510AL
FDA Devices Moderate Jan 6, 2021

Covidien TA Auto Suture Vascular Loading Unit with DST Series Technology 30 mm- V3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3L
FDA Devices Moderate Jan 6, 2021

Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3S
FDA Devices Moderate Dec 9, 2020

Capnostream 35 Portable Respiratory Monitor, Product numbers PM35MN02, PM35MN01, PM35MN05, DLPM35MN02 - Product Usage: use during both no motion and motion conditions and for patients who are well or poorly perfused.
FDA Devices Moderate Nov 18, 2020

Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for use on patient population sizes from Neonatal (NICU) through Adult who require respiratory support or mechanical ventilation SKU: 980X1ENDIUU 980X1ENDIUU 980X3FRAIQC 980X3DEDRAC 980X3ENNISB 980X3NLDRAC 980X3PLDIPC 980X3ESDIEC 980X3ITDIEC 980X3JADIJJ 980X3SVAIQC 980U3ENASAA 980U1ENDICU 980U1FRDICU 980X3ENDRAC 980X1FRDISS 980A3ENNISB 980X1PLDIPC 980X3SKNISC 980U3ESDIUU 980X1DEDISS 980X3DEDISS 980X3HUNISC 98

Covidien LLC carries an outsized archive share

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

Frequently Asked Questions

How many federal recall notices name Covidien LLC? ▼
PlainRecalls indexes 340 distinct federal recall events naming Covidien LLC, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Covidien LLC sit among other recalling firms? ▼
Covidien LLC ranks #28 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Covidien LLC's notices? ▼
FDA Devices accounts for 340 of this firm's 340 indexed notices.
What product category dominates Covidien LLC's filing book? ▼
Filings for Covidien LLC 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 LLC: 340 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 LLC; individual notices remain authoritative on each linked recall page.

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