FDA Medical devices recall ·
Baxter Operating table TruSystem 7000 U (MB), Product codes: a) recall
- Recall number
- Z-0210-2025
- Date
- (initiated September 19, 2024)
- Company / brand
- Baxter Healthcare Corporation
1 Baxter Pkwy, Deerfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 6045 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633
Why was it recalled?
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
a) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS
Distribution
Worldwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0210-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.