Cme America LLC
Country not established
- Devices
- 141
- FDA recalls
- 48
Catalogue
Search and filter all 141 devicesShowing 51-100 of 141
Company details
- DUNS number
- 002125419
- [email protected]
- Phone
- 303-936-4945
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 1
- 2020 46
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2020
- 30 Jul 2020 Z-0525-2021 Class II Terminated Multiple reasons:
1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated.
2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Full distribution text
- 30 Jul 2020 Z-0526-2021 Class II Terminated Multiple reasons:
1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated.
2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Full distribution text
- 30 Jul 2020 Z-0527-2021 Class II Terminated Multiple reasons:
1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated.
2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Full distribution text
- 30 Jul 2020 Z-0528-2021 Class II Terminated Multiple reasons:
1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated.
2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Full distribution text
- 30 Jul 2020 Z-0529-2021 Class II Terminated Multiple reasons:
1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated.
2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Full distribution text
- 30 Jul 2020 Z-0530-2021 Class II Terminated Multiple reasons:
1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated.
2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Full distribution text
- 16 Jun 2020 Z-2553-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2554-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2555-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2556-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 30 Jul 2020 Z-0525-2021 Class II Terminated Multiple reasons:
1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated.
2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Show the 25 most recent of 48 recalls
2020
- 16 Jun 2020 Z-2557-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2558-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2559-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2560-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2561-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2562-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2563-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2564-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2565-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2566-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2567-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2568-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2569-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2570-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2571-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Full distribution text
- 16 Jun 2020 Z-2557-2020 Class I Terminated Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy