AVE 2 Birthing Bed — Class II medical device recall Z-0991-2019
Terminated recall by Linet Spol. S.r.o., reported 2019-03-20, distributed in AL, AZ, CA, CO, CT, DE, FL, IL…. LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cab
| Recall number | Z-0991-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Linet Spol. S.r.o., Slany, N/A, Czech Republic |
| Recall initiated | 2019-01-07 |
| Classified | 2019-03-08 |
| Reported by FDA | 2019-03-20 |
| Terminated | 2023-05-31 |
| Distributed | AL, AZ, CA, CO, CT, DE, FL, IL, KS, KY, LA, MN, MO, NJ, OH, OK, OR, TN, TX, UT, WA |
| Quantity | 253 devices |
| Reason classes | device malfunction |
| Serial numbers | 4PPB0091 |
Product
AVE 2 Birthing Bed
Reason for recall
LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cable breaking at the bed connection or the orange insulation of the power cable may fail causing a possible spark or possible exposure to a live conductor.
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-0991-2019. 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.