Drug recall
Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be used by end users who are eighteen (18)…
FDA recall event 75177 · Class II · A & D Enginering Inc
Key facts
| Event ID | 75177 |
|---|---|
| Recall numbers | Z-0063-2017 |
| Recalling firm | A & D Enginering Inc |
| Product type | Devices |
| Products | Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be used by end users who are eighteen (18) years and older at home to monitor their blood pressure (systolic and diastolic) and pulse… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A&D may have shipped blood pressure monitors that were not labeled for use with small cuff. |
| Initiation date | Sep 12, 2016 |
| Report date | Oct 19, 2016 |
| Termination date | Aug 28, 2018 |
| City | San Jose |
| State | CA |
| Country | United States |
| FEI number | 2082313 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: