FDA Device recall Z-0991-2019
AVE 2 Birthing Bed
- FDA Device
- Class II
- terminated
- Published 2019-03-20
On 2019-03-20 the FDA classified a Class II recall of AVE 2 Birthing Bed by Linet Spol S R O, citing 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 pow….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0991-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-01-07 |
| Published | 2019-03-20 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Linet Spol S R O |
| Distribution | AL, AZ, CA, CO, CT, DE, FL, IL, KS, KY, LA, MN, MO, NJ, OH, OK, OR, TN, TX, UT, WA |
Product
AVE 2 Birthing Bed
Reason
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.
Identifiers
| code_info | Serial Numbers 4PPB0091 through 4PPB626 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0991-2019%22
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