FDAFDA · Food and drugs·Recall number Z-0884-2025
Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
Published January 22, 2025 · Recall initiated: December 20, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- US, Nationwide Distribution
- Lot
- UDI/DI 00887761978201, Serial Numbers: 124080000663, 124020000164, 124020000165, 124020000166, 124020000167, 124020000168, 124020000169, 124020000170, 124020000171, 124020000172, 124020000173, 124020000174, 124020000175, 124020000176, 124080000659, 124080000661, 124080000662, 124080000666, 124080000667, 124080000668, 124080000669, 123420000499, 123490000931, 124010000910, 124020000163, 124080000670, 124080000672, 124080000673, 124080000675, 124080000677, 124080000678, 124080000679, 124080000715, 124080000716, 124080000718, 124080000733, 124080000735, 124080000772, 124080000784, 124080000854, 124080000855, 124080000856, 124080000857, 124080000863, 124080000865, 124080000919, 124080000920, 124080000921, 124080000922, 124080000923, 124080000924, 124080000925, 124080000926, 124080001290, 124080001367, 124080001388, 124080001409, 124080001594, 124080001596, 124080001601, 124080001602, 124080001603, 124080001604, 124080001605, 124080001606, 124080001608, 124080001609, 124080001610, 124080001612, 124080001614, 124140000062, 124140000063, 124140000065, 124140000067, 124140000068, 124140000069, 124140000070, 124140000123, 124140000125, 124140000126, 124140000127, 124140000401, 124140000402, 124140000403, 124140000404, 124140000405, 124140000636, 124140000637, 124140000638, 124140000668, 124140000671, 124140000672, 124140000675, 124140000677, 124140000679, 124140000681, 124140000683, 124140000684, 124140000686, 124140000687, 124140000688, 124140001005, 124140001014, 124140001187, 124140001191, 124140001195, 124140001201, 124140001203, 124160001584, 124170000747, 124170000749, 124170000804, 124170000828, 124170000832, 124170001158, 124170001159, 124170001161, 124170001162, 124170001163, 124170001166, 124170001171, 124170001172, 124200000070, 124200000071, 124200000072, 124200000073, 124200000074, 124200000076, 124200000077, 124200000078, 124200000079, 124200000080, 124200000081, 124200000083, 124200000084, 124200002473, 124200002474, 124200002475, 124200002476, 124200002478, 124200002479, 124200002480, 124200002481, 124200002482, 124200002485, 124200002486, 124200002489, 124200002490, 124200002491, 124200002492, 124200002493, 124200002494, 124200002495, 124200002496, 124200002497, 124200002498, 124200002499, 124200002500, 124200002501, 124200002502, 124200002503, 124200002504, 124200002505, 124200002506, 124200002507, 124200002508, 124200002509, 124250000491, 124250000492, 124250000493, 124250000494, 124250000495, 124250000496, 124250000497, 124250000498, 124250000499, 124250000500, 124250000533, 124250000534, 124250000535, 124250000536, 124250000537, 124250000538, 124260000558, 124260001171, 124280000585, 124280000741.
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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