Alere San Diego, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1702-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Abbott Cholestech LDX Battery Kit, Model: 3LP656194-PCM-LD, PN: 55170

Product Classification:

Class II

Date Initiated: March 1, 2024

Date Posted: May 8, 2024

Recall Number: Z-1702-2024

Event ID: 94190

Reason for Recall:

There is a potential that the Cholestech LDX battery (an external battery pack available as an optional accessory to the Cholestech LDX Analyzer) may swell which could cause minor burns, cuts or abrasions, or low current electrical shock to the user.

Status: Ongoing

Product Quantity: 559 units

Code Information:

All Lots/ UDI:

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of United Kingdom, Netherlands and Kenya.

Voluntary or Mandated:

Voluntary: Firm initiated