Covidien Recalls
493 recalls on record · June 27, 2012 to August 19, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
Also filed under
The recall feeds record what looks like the same company under more than one name:
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980X1JADIJJ
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980X1ENNISB
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980X1ENDIUU
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980X1ENDIPC
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator,980X1ENAIQC
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980U3ESDIUU
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980U1ESDIUC
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980U1ENASAA
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980S3ENDICU
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980S1ENDICU
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980A3ENNISB
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980A1ENNISB
Hazard: Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
December 15, 2021Medical DevicesFDA
Covidien Llc recalls Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information o
Hazard: Intermittent risk of electric shock to users if an affected charger is used in conjunction with a faulty or bypassed institutions Mains Protective Earth (Ground) circuit
November 17, 2021Medical DevicesFDA
Covidien Llc recalls Covidien Emprint Ablation Catheter with Thermosphere Technology Bronchoscopic Ablation, CFN CA108L1
Hazard: The firm identified an error in the device temperature monitoring circuitry which is designed to interrupt energy delivery in the event of a primary cooling system failure. Use of an affected device in conjunction with a primary cooling system failure could lead to the applicator tip overheating and associated heat damage which could result in an allergic/toxic reaction, unintended tissue ablation, tissue burn, and/or a delay of treatment while an alternate device is located.
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 55 cm, Item Code 8888
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 44 cm, Item Code 8888
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 33 cm, Item Code 8888
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 28 cm, Item Code 8888
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 23 cm, Item Code 8888
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 19 cm, Item Code 8888
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Repair Kit 15 FR TAL 55cm, Sterile, Item Code 8888541155
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Repair Kit 15 FR TAL 44cm, Sterile, Item Code 8888541144
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Repair Kit 15 FR TAL 33cm, Sterile, Item Code 8888541133
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Repair Kit 15 FR TAL 28cm, Sterile, Item Code 8888541128
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Repair Kit 15 FR TAL 23cm, Sterile, Item Code 8888541123
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Repair Kit 15 FR TAL 19cm, Sterile, Item Code 8888541119
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 55cm, Item Code 8888541055
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 44cm, Item Code 8888541044
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 33cm, Item Code 8888541033
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
September 8, 2021Medical DevicesFDA
Covidien, LP recalls Palindrome RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 28 cm, Item Code 8888541028
Hazard: This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).