AVE 2 Birthing Bed — Class III medical device recall Z-2781-2020
Ongoing recall by Linet Americas, reported 2020-08-19, distributed nationwide. The UDI on the device label indicates incorrect manufacturer.
| Recall number | Z-2781-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Linet Americas, Charlotte, NC, United States |
| Recall initiated | 2020-03-06 |
| Classified | 2020-08-12 |
| Reported by FDA | 2020-08-19 |
| Distributed | Nationwide (US) |
| Quantity | 202 devices |
| Reason classes | labeling |
| Lot numbers | PPB1155, PPB1174, PPB1194, PPB1213, PPB1222, PPB1241, PPB1265, PPB1284, PPB1292, PPB1311, PPB1346, PPB1365, PPB1375, PPB1394, PPB1446, PPB1449, PPB1451, PPB1466, PPB1477, PPB1496, PPB1508, PPB1527, PPB1541, PPB1542 |
| Model numbers | 4BCPPB-3XCZ0002, 4BCPPB-BCZ0009, 4BCPPB-CCZ0008 |
Product
AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also as aid to search for individual positions providing relief in all delivery stages including postpartum period. Birthing bed is not intended for use as a general hospital bed.
Reason for recall
The UDI on the device label indicates incorrect manufacturer.
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-2781-2020. 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.