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, 2015

Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 33cmItem Code: 8888145065CP
FDA Devices Moderate Jul 8, 2015

Palindrome HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888133509
FDA Devices Moderate Jul 8, 2015

Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888145062P
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888145065
FDA Devices Moderate Jul 8, 2015

Palindrome Precision SI Chronic Catheter Kit 14.5 Fr x 55cm Item Code: 8888145066CP
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Sport Pack 14.5 Fr x 28 cm Item Code:8888228458
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Kit 14.5 Fr x 55cm Item Code: 8888145066C
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 23cm Item Code: 8888145063
FDA Devices Moderate Jul 8, 2015

Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888145050C
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888145062C
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888128458
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 23cm Item Code: 8888145063C
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888145064C
FDA Devices Moderate Jul 8, 2015

Palindrome Precision SI Chronic Catheter Kit 14.5 Fr x 55cm Item Code: 8888145066CP
FDA Devices Moderate Jul 8, 2015

Palindrome SI Chronic Catheter Kit 14.5 Fr x 28cm Item Code: 8888245064
FDA Devices Moderate Jul 8, 2015

Palindrome Precision SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888133508P
FDA Devices Moderate Jul 8, 2015

Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888145049
FDA Devices Moderate Jul 8, 2015

Palindrome Precision HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888145050P
FDA Devices Moderate May 20, 2015

VenaSeal, Sapheon Closure System, Model # SP-101, VS-301 and VS-402. For vascular use.
FDA Devices Critical Oct 22, 2014

Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-connected Part Number: 22660PC
FDA Devices Critical Oct 22, 2014

Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R
FDA Devices Critical Oct 22, 2014

Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
FDA Devices Critical Oct 22, 2014

MediChoice¿ Multifunction Electrode Part Number: MC171 OH
FDA Devices Critical Oct 22, 2014

Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A
FDA Devices Critical Oct 22, 2014

Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660
FDA Devices Moderate Jul 16, 2014

Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended to provide padding under the patient, and help maintain the position of an anesthetized patient during surgery.
FDA Devices Moderate Sep 18, 2013

Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881580123 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill Product ID: 8881570121 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881590125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881590123 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881580125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID: 8881590121 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 3 mL Fill Product ID: 8881570123 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 5 mL Fill Product ID: 8881570125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Moderate Sep 18, 2013

Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID:8881580121 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
FDA Devices Low May 22, 2013

Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit.
FDA Devices Low May 22, 2013

Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit.
FDA Devices Moderate May 8, 2013

Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Product ID: 22550P. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.
FDA Devices Moderate May 8, 2013

Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.
FDA Devices Moderate Sep 26, 2012

HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien) 540 Oakmead Parkway Sunnyvale, CA 95085. The HALO Flex Energy Generator is indicated for use for the coagulation of soft tissue. The HALO Flex System is indicated for use in the coagulation of bleeding and non-bleeding sites in the gastrointestinal tract including but not limited to, the esophagus, including Barrett's Esophagus.

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