Cme America LLC
Country not established
- Devices
- 141
- FDA recalls
- 48
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 141 devicesShowing 1-50 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
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- 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
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- 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
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- 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
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- 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
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- 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
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- 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
Frequently asked questions
How many devices does CME AMERICA LLC have in the registry?
The registry currently lists 141 devices for CME AMERICA LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list CME AMERICA LLC's devices?
Among its 50 most recently registered devices, CME AMERICA LLC has devices listed in FDA GUDID (50 devices).
What risk classes do CME AMERICA LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for CME AMERICA LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for CME AMERICA LLC?
FDA recall records list 48 recalls initiated by CME AMERICA LLC, the most recent initiated on 30 Jul 2020. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from CME AMERICA LLC in the registry?
The most recently registered devices listed for CME AMERICA LLC include BodyGuard® Microset A120-160XPS, Refurbished BodyGuard 121 Twins Pump 100-105TSAR, BodyGuard® Syringe Microset A120-161XYB and Standard BodySet® with Needleless Connectors A120-125XSE.