Covidien LLC: 92 recalls on record

Recalls filed with 1 agency: FDA (92).

First recall on record: September 26, 2012. Most recent: August 26, 2026.

Risk classification: Class I: 11 · Class II: 79 · Class III: 2

Most recent recalls

DateAgencyProduct
October 22, 2014FDAMediChoice¿ Multifunction Electrode Part Number: MC171 OHZ-0047-2015
October 22, 2014FDACoviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-connected …Z-0044-2015
July 16, 2014FDADevon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Prod…Z-1997-2014
September 18, 2013FDAMonoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 88815…Z-2185-2013
September 18, 2013FDAMonoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 3 mL Fill Product ID: 88…Z-2179-2013
September 18, 2013FDAMonoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID: 8881…Z-2184-2013
September 18, 2013FDAMonoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 5 mL Fill Product ID: 88…Z-2180-2013
September 18, 2013FDAMonoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID:888158…Z-2181-2013
September 18, 2013FDAMonoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 888158…Z-2182-2013
September 18, 2013FDAMonoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill Product ID: 8…Z-2178-2013
September 18, 2013FDAMonoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 88815…Z-2186-2013
September 18, 2013FDAMonoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 888158…Z-2183-2013
May 22, 2013FDACurity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. I…Z-1303-2013
May 22, 2013FDACurity Staple Remover Kit; Product Code: 66701. Staple Remover Kit.Z-1304-2013
May 8, 2013FDAMedi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. …Z-1184-2013
May 8, 2013FDAMedi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Product ID: 22550…Z-1185-2013
September 26, 2012FDAHALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien) 540 Oakmead …Z-2379-2012

Questions about this company

How many recalls does Covidien LLC have?
Recalert has 92 U.S. recalls on record for Covidien LLC, published between September 26, 2012 and August 26, 2026.
Which agencies have handled Covidien LLC recalls?
Covidien LLC appears as the recalling firm in recalls from: FDA (92).

Do you carry products from Covidien LLC? Check your whole catalog free against 80,000+ recalls.

Paste up to 100 UPCs or SKUs and see which ones match a CPSC, FDA, NHTSA or FSIS recall. No account needed.

Check my catalog free

Want it checked every night instead? Starter watches 500 SKUs for $29/month. See plans

Related companies