FDA Medical devices recall ·

Battery Charging Station recall

Recall number
Z-1587-2026
Date
(initiated February 6, 2026)
Company / brand
Datascope Corp.
1300 Macarthur Blvd, Mahwah, NJ, United States
Category
Medical devices › Class III
Classification
Class III
Status
Ongoing
Units affected
28 units (20 US, 8 OUS)
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

Product

Battery Charging Station; Model: 0998-00-0802;

Why was it recalled?

The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.

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

Model: 0998-00-0802; UDI: 10607567111964; Serial Numbers: 200019347EAI, 200019847EAI, 200019447EAI, 210018625EAI, 210017925EAI, 210017525EAI, 210018425EAI, 210020144EAI, 210020944EAI, 210022544EAI, 210020244EAI, 210022144EAI, 210020044EAI, 210020544EAI, 210021344EAI, 210023244EAI, 210018025EAI, 210019025EAI, 210021144EAI, 210021044EAI, 210022344EAI, 210019225EAI, 210019125EAI, 210018525EAI, 210022844EAI, 200017647EAI, 210019725EAI, 210022744EAI;

Distribution

Worldwide - US Nationwide distribution in the states of FL, DC, GA, IL, IN, MD, MI, NC, TX, WA, WI and the countries of Australia, Hong Kong, Israel, Japan, Norway.

States: District of Columbia Florida Georgia Illinois Indiana Maryland Michigan North Carolina Texas Washington Wisconsin

What does Class III mean?

Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).

Source: FDA (medical devices), recall Z-1587-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.