Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2781-2020 — 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.

U.S. FDA — Device Enforcement · United States · 2020-03-06 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2781-2020
Date of alert: 2020-03-06
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Linet Americas
Product category: device
Product type: Devices

Reported risk: The UDI on the device label indicates incorrect manufacturer.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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