Blood Pressure Monitor UA-767PBT-Ci for small cuff — Class II medical device recall Z-0063-2017
Terminated recall by A & D Enginering Inc, reported 2016-10-19, distributed in MA, NY, TX, VA. A&D may have shipped blood pressure monitors that were not labeled for use with small cuff.
| Recall number | Z-0063-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | A & D Enginering Inc, San Jose, CA, United States |
| Recall initiated | 2016-09-12 |
| Classified | 2016-10-09 |
| Reported by FDA | 2016-10-19 |
| Terminated | 2018-08-28 |
| Distributed | MA, NY, TX, VA |
| Quantity | 378 units |
| Reason classes | labeling |
| Serial numbers | 5140601121, 5140601122, 5140601123, 5140601124, 5140601125, 5140601126, 5140601127, 5140601128, 5140601129, 5140601130, 5140601191, 5140601192, 5140601193, 5140601194, 5140601195, 5140601196, 5140601197, 5140601198, 5140601199, 5140601200, 5140800481, 5140800482, 5140800483, 5140800484, 5140800485 and 352 more |
Product
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 rate.
Reason for recall
A&D may have shipped blood pressure monitors that were not labeled for use with small cuff.
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-0063-2017. 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.