Alaris Pump Module, Model 8100, serviced/repaired by Step-Har Medical with an impacted bezel repair part
FDA device recall Z-1543-2021 · posted 2021-05-10 · Terminated
Recall details
- Recalling firm
- STEP-HAR MEDICAL LLC
- Reason for recall
- 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.
- Action taken
- On 02/26/2021, the one customer was notified of the recall via phone call and email. On 04/15/21, a Voluntary Field Safety Corrective Action notice were mailed. The firm asked their customer to respond so the bezel repair part could be replaced. Customers can contact the recalling firm at: 657-267-0054 or stdoan@stepharmedical.com
- Root cause
- Component design/selection
- Status
- Terminated
- Product code
- FRN
- Quantity affected
- 2
- Distribution
- IA
- Date initiated
- 2021-02-26
- Date posted
- 2021-05-10
- Date terminated
- 2024-08-15
- Location
- Fountain Valley, CA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ALARIS SYSTEM WITH GUARDRAILS SUITE MX (K133532) | Carefusion 303, Inc. | 2014-08-21 |