Facility

Getinge Group Logistics America, LLC

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)	3025504317
Establishment type	Repack or Relabel Medical Device
Location	160 Princeton Highstown Road E Windsor, NJ, US 08520
Registration status	Active · expires 2026
Parent company	Getinge (owner-operator 10055718)
Brand names	Maquet PowerLED

Activity by year

Recalls (1)

Devices registered here (2)

Light, Surgical, Ceiling Mounted
Product code FSY (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4580
Lamp, Surgical
Product code FTD (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4580

Recalls & enforcement

Class IITerminated2021-04-15
There is a potential for abnormal inflation of the mattress.

All facilities operated by Getinge

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. “Getinge Group Logistics America, LLC (FEI 3025504317) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3025504317-getinge-group-logistics-america-llc/

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