Covidien Recalls
336 recalls on record in the United States
Covidien LLC recalls Signia" Power Handle (SIGPHANDLE, SIGNVAL1 and SIGVAL20 - Ki
Product reportedly shutting down during use.
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Covidien LLC recalls Rechargeable Li-ion battery used with Puritan Bennett TM 980
Rechargeable lithium-ion batteries with incorrect firmware that are used in certain Puritan Bennett 980 ventilators may not fully charge after installation.
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Covidien LLC recalls Situate Gauze RF and X-Ray detectable. Product Number: G080
This voluntary recall is being conducted due to the potential for failure to detect the affected Situate" gauze - RF and Xray detectable products by the Situate" detection console due to a manufacturing error.
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Covidien LLC recalls Endo GIA" Radial Reload with Tri-Staple" Technology The E
The device cartridge disengaged during use due to manufacturing error.
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Covidien LLC recalls GastriSail" Gastric Positioning Device Product Usage: The
Reports of gastric or esophageal perforation occurring in procedures where the GastriSail" Gastric Positioning device has been used.
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Covidien LLC recalls Endo GIA Auto Suture Universal Articulating Loading Unit for
Potential for failure of the device safety interlock. The safety interlock prevents an empty single-use loading unit from being fired a second time.
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Covidien LP recalls Covidien Vistec" X-Ray Detectable Sponges, 7317 Vistec" X-Ra
Medtronic is voluntarily recalling two production lots of its Covidien Vistec" x-ray detectable sponges de to possible contamination with human blood caused by handling of the product during the manufacturing process and prior to final packaging and Ethylene Oxide sterilization.
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Covidien LLC recalls Covidien Emprint Percutaneous Antenna with Thermosphere Tech
The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.
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Covidien LLC recalls Covidien Emprint Percutaneous Antenna with Thermosphere Tech
The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.
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Covidien LLC recalls Covidien Emprint Percutaneous Antenna with Thermosphere Tech
The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.
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Covidien LLC recalls Covidien Emprint Percutaneous Antenna with Thermosphere Tech
The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.
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Covidien LLC recalls Covidien Emprint Percutaneous Antenna with Thermosphere Tech
The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.
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Covidien LLC recalls Covidien Emprint Percutaneous Antenna with Thermosphere Tech
The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.
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Covidien LLC recalls Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item C
Cotton tip of the device may disengage due to insufficient adhesive
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COVIDIEN MEDTRONIC recalls Valleylab Laparoscopic Handset; Material # E2750; Laproscopi
Customer reports of the device handset continuing to operate after release of the activation button.
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Covidien LLC recalls Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm), St
Product sterility is compromised due to breach of sterile barrier
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Covidien LLC recalls Covidien Curity Eye Pad Item Code: 91650 The sterile eye
Product sterility is compromised due to breach of sterile barrier
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Covidien LLC recalls Covidien Curity Eye Pad Item Code: 03201 The sterile eye
Product sterility is compromised due to breach of sterile barrier
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Covidien LLC recalls Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm), St
Product sterility is compromised due to breach of sterile barrier
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Covidien LLC recalls Covidien Curity Eye Pad Oval, 1-5/8 x 2-5/8 (4.2 cm x 6.7
Product sterility is compromised due to breach of sterile barrier
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Covidien LLC recalls Covidien Kerlix Super Sponge Saline Dressing, Sterile Item
Product sterility is compromised due to breach of sterile barrier
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Covidien LLC recalls Covidien Curity Sodium Chloride Dressing , 6 x 6-3/4 (15
Product sterility is compromised due to breach of sterile barrier
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Covidien LLC recalls Premier Guard Drape, Sterile. For Use with Verisphere (01-0
Sterility compromised due to breach in sterile barrier
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Covidien LLC recalls Premier Guard Sterile Drape For Use with Blair-Port Wand (02
Sterility compromised due to breach in sterile barrier
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Covidien LLC recalls Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; T
Labeling error: The label indicates the product is latex free, but the headband component included with the forehead sensor does contain latex.
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Covidien, LP recalls Covidien Signia" Small Diameter Curved Tip Intelligent Reloa
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
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Covidien, LP recalls Covidien Signia" Small Diameter Curved Tip Intelligent Reloa
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
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Covidien recalls Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF
Bedside SpO2 Patient Monitoring System alarms not heard/recognized, resulting in: treatment delay, lack of low oxygen saturation response, respiratory failure, arrhythmia. Highlighting operator's manual: 1)For patient Safety don't silence/decrease alarm volume, 2)Sensor off alarm (no perfusion detected) is low priority alarm, 3)Set monitors to Homecare Mode outside of hospital/professional setting
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Covidien recalls Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70
Ventilator Printed Circuit Board Assembly may have two separate capacitors that may fail, which may result in the ventilator either shutting down during use, thus necessitating use of an alternate form of ventilation, or the shutdown alert alarm fails to alarm effectively during shut down, which may result in respiratory failure, hypoventilation, low oxygen saturation, hypoxia, treatment delay.
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Covidien recalls Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff
Tracheostomy tube with cuff reusable inner cannula has a flange that may disconnect from the outer cannula of the device, which could cause respiratory failure, aspiration, unspecified tissue injury, aspiration, respiratory tract infection, bronchospasm, a delay to treatment and/or death.
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Showing 30 of 336 recalls. See all →