PlainRecalls

Covidien LLC

Compiled from official public sources by the editorial team.

335 recalls on record · Latest: Mar 18, 2026

Covidien LLC Recall Insight

Covidien LLC appears on 335 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.329% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Mar 18, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 35 entries, severity tagging shows 6 critical, 27 moderate, and 2 lower-severity recalls. Affected-unit counts are disclosed on 35 of 35 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (35). The date window on this page runs from Sep 26, 2012 to Jul 8, 2015.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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 …

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 syri…

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…

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 s…

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 syr…

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 syri…

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 sy…

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 …

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 …

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 syri…

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 monitor…

FDA Devices Moderate May 8, 2013

Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardioversion, pacing, ECG monitoring,…

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 Genera…

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.