FreshRecalls

Covidien recalls

6 recent recalls on record for Covidien in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.

Models with recalls

COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code (1)Covidien EndoStitch" Polysorb Single Use Loading Unit (1)Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF (1)Covidien Mon-a-Therm General Purpose Temperature Probe REF (1)Covidien Mon-a-Therm general purpose temperature probe size (1)Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code (1)

All Covidien recalls

FDA Class II · Medical device · July 8, 2026

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code recall — Covidien LLC

Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.

Official ID Z-2653-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien EndoStitch" Polysorb Single Use Loading Unit recall — Covidien, LP

The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.

Official ID Z-2281-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien Mon-a-Therm general purpose temperature probe size recall — Covidien LLC

Temperature probe devices lack FDA clearance.

Official ID Z-2273-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien Mon-a-Therm General Purpose Temperature Probe REF recall — Covidien LLC

Temperature probe devices lack FDA clearance.

Official ID Z-2272-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF recall — Covidien LLC

Temperature probe devices lack FDA clearance.

Official ID Z-2271-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code recall — Covidien LLC

Due to customer complaint regarding incorrect display box labeling.

Official ID Z-2261-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.