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

Recall Z-1816-2025 — Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E100436, P3700E100437, P3700E100438, P3700E100439, P3700E100441, P3700E100442, P3700E100443, P3700E100444, P3700E100445, P3700E100446, P3700E100448, P3700E100449, P3700E100450, P3700E100

U.S. FDA — Device Enforcement · United States · 2025-05-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1816-2025
Date of alert
2025-05-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00887761000896
Reported risk: There is a potential for improper crimps on the signal wires of the actuators which could result in a loss of ability to lower the bed or the foot section of the bed.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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