Welch Allyn Life2000 Ventilation System recall
Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A, 3) BT-20-0002AP, 4) BT-20-0007…
Why was Welch Allyn Life2000 Ventilation System recalled?
The Life2000 ventilator may fail to initiate the Low Gas Pressure alarm if the pressure gas source (Life2000 compressor, oxygen cylinder or wall source) is not supplied to the ventilator before initiating therapy.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 00887761978089 or 00815410020537, All Life2000 Ventilators with software version 06.08.00.00
- Product
- Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A, 3) BT-20-0002AP, 4) BT-20-0007…
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 10,957 units
- Distribution
- US nationwide distribution.
- Recall date
- October 30, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)