Fresh Recalls

Covidien recalls

12 recent recalls on record for Covidien in connected official government data as of October 22, 2026 at 6:00 PM 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)Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU (1)EndoFLIP System that includes (1)Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX (1)Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 (1)V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY P (1)V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 G (1)

All Covidien recalls

FDA Class II · Medical device · August 26, 2026

EndoFLIP System that includes recall — Covidien, LLC

The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.

Official ID Z-2950-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Official ID Z-2922-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Official ID Z-2921-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Official ID Z-2920-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY P recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Official ID Z-2919-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 G recall — Covidien, LP

Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…

Official ID Z-2918-2026 · Official record ↗

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 October 22, 2026 at 6:00 PM UTC.