[Recalled] Abbott Cholestech LDX Battery Kit, Model: 3LP656194-PCM-LD, PN: 55170 — There is a potential that the Cholestech LDX battery (an external battery pack… | FDA 2024-03-01
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Abbott Cholestech LDX Battery Kit, Model: 3LP656194-PCM-LD, PN: 55170 |
|---|---|
| Brand / manufacturer | Alere San Diego, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1702-2024 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 01 March 2024 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Alere San Diego, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.