FDA Device recall Z-2204-2021
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted bezel repair part TI…
- FDA Device
- Class I
- terminated
- Published 2021-08-18
On 2021-08-18 the FDA classified a Class I recall of Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted bezel repair part TI… by Biomedical Equipment Service Bmes, citing bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2204-2021 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2021-02-25 |
| Published | 2021-08-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Biomedical Equipment Service Bmes |
| Distribution | CA, IL, IN, KY, LA, NJ, NV, OH, PA |
Product
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted bezel repair part TIPA-8100-4410
Reason
Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.
Identifiers
| code_info | Serial Numbers: 13414138 13414659 13414829 13415843 15221825 15221825 12744341 12835089 12861990 12875918 12959808 1307…Serial Numbers: 13414138 13414659 13414829 13415843 15221825 15221825 12744341 12835089 12861990 12875918 12959808 13077410 13077413 13077474 13681407 15306396 15306899 12420646 12421169 12635894 12781498 12949510 13367664 13415216 13931954 2000189 3000595 3000883 3060800 3114560 3163062 3169497 3704252 3704268 3704322 3704343 3704366 3704476 3704477 3704485 3704529 3704536 3704549 3704639 3704645 3704810 3704814 3704853 4109720 4110277 8000560 9885878 9923593 9923615 9923671 9923800 9928207 13900270 13895113 13895704 10938662 12335127 12356902 12357956 12371188 12377005 12377451 12377463 12377633 12377809 12377870 12378093 12378095 12378248 12378686 12379004 12435805 12447105 12447140 12447792 12447797 12447834 12447943 12457014 12527904 12534361 12558945 12559059 12560637 12569213 12609470 12609853 12610581 12610619 12610636 12610848 12611472 12612154 12612168 12612237 12612426 12612541 12612616 12612728 12612766 12613011 12613031 12613120 12613277 12613768 12613837 12613890 12619413 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2204-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.