Covidien, LLC recalls
15 recalls filed under Covidien, LLC. The most recent was published August 26, 2026.
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Class II · 2 months ago
Covidien, LLC EndoFlip System that includes: Endoflip 1 System EF-100 05391530810050 recall: The system's 24-hour usage limit results in catheters incorrectly flagged
The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.
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Class II · 2 months ago
Covidien, LP Dermalon 88861757-31 Dermalon* 4-0 BLU 75CM C13 88861757-31 88861799-31 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Covidien, LP Surgipro SP-623 Surgipro* 2-0 BLU 75CM SC2 X36 SP-623 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Covidien, LP V-Loc 90 Absorbable Wound Closure Device Vloc 90 0 VL 22 GS-21 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Covidien, LP Surgipro II S8698GX Surgipro II BL 5/0 18 P-13 S8698GX recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Covidien, LP V-Loc 180 Absorbable Wound Closure Device BOX Bedside Stapling IS King recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 4 months ago
Covidien Shiley Disposable Decannulation Plug REF Ddcp Udi-Di code recall: Due to product labeling incorrectly including the symbol indicating non-DEHP
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.
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Class II · 5 months ago
Covidien EndoStitch" Polysorb Single Use Loading Unit recall: The presence of holes in the pouch may compromise the package s ability
The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental…
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Class II · 5 months ago
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor recall: Temperature probe devices lack FDA clearance
Temperature probe devices lack FDA clearance.
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Class II · 5 months ago
Covidien Mon-a-Therm General Purpose recall: Temperature probe devices lack FDA clearance
Temperature probe devices lack FDA clearance.
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Class II · 5 months ago
Covidien Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN recall: Due to customer complaint regarding incorrect display box labeling
Due to customer complaint regarding incorrect display box labeling.
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Class II · 5 months ago
Covidien Mon-a-Therm general purpose recall: Temperature probe devices lack FDA clearance
Temperature probe devices lack FDA clearance.
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Class II · 7 months ago
Covidien LLC HealthCast "Vital Sync" Remote Patient Monitoring System which consists recall: Due to complaints and investigations stating that alarms from the primary
Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on…
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Class II · 11 months ago
Covidien Signia" Small Diameter Curved Tip Intelligent Reload recall: A manufacturing issue could lead to a malformed cover tube press
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the…
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Class II · 11 months ago
Covidien Signia" Small Diameter Curved Tip Intelligent Reload recall: A manufacturing issue could lead to a malformed cover tube press
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the…
About this page
Covidien, LLC appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.