Maquet XS Flat Screen Monitor Holder — Class II medical device recall Z-0989-2019
Terminated recall by GETINGE US SALES LLC, reported 2019-03-13, distributed in AZ, TX. The affected flat screen monitor holders might not be compliant with grounding requirements. As a consequence,
| Recall number | Z-0989-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GETINGE US SALES LLC, Wayne, NJ, United States |
| Recall initiated | 2019-01-08 |
| Classified | 2019-03-07 |
| Reported by FDA | 2019-03-13 |
| Terminated | 2020-06-03 |
| Distributed | AZ, TX |
| Quantity | 6 |
| Serial numbers | 500001, 500002, 500003, 500004, 500005, 500006 |
| Model numbers | ARD268400150A |
Product
Maquet XS Flat Screen Monitor Holder, PWD70+DF HD R XS32 K3 SPE, Configuration Part Number ARD268400150A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
Reason for recall
The affected flat screen monitor holders might not be compliant with grounding requirements. As a consequence, there is a risk of mild to severe/fatal electric shock under certain conditions while using the flat screen monitor holder with voltage of 100-220V.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0989-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.