Facility

Bridge to Life Ltd

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3031884833
Establishment type	Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Location	3300 Breckinridge Blvd., Suite 200 Duluth, GA, US 30096
Registration status	Active · expires 2026
Parent company	Bridge to Life Ltd. (owner-operator 10038889)
Brand names	EasiSlush

Activity by year

Recalls (1)

Devices registered here (2)

System, Perfusion, Kidney
Product code KDN (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5880
Set, Perfusion, Kidney, Disposable
Product code KDL (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5880

Recalls & enforcement

Class IIOngoing2025-06-12
The firm issued a field safety notice after becoming aware of three lots of products not having quarterly dose audits being completed on time in the first quarter of 2024. Routine lot by lot testing was completed properly however the quarterly dose audit (sampling/testing to mon…

All facilities operated by Bridge to Life Ltd.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Bridge to Life Ltd (FEI 3031884833) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3031884833-bridge-to-life-ltd/

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