Facility

Little Rapids Corporation

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

Key facts

1recalls · worst Class II

2inspections · worst VAI

—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)	1000049086
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	2273 Larsen Rd GREEN BAY, WI, US 54303
Registration status	Active · expires 2026
Parent company	LITTLE RAPIDS CORP. (owner-operator 2182303)
Brand names	Graham Professional; Graham Medical

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Tourniquet, Nonpneumatic
Product code GAX (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.5900

Recalls & enforcement

Class IITerminated2017-12-27
The secondary supplier provided material was within specification but did not meet our design needs compared to the primary manufacturer. The product is designed for patient transfer, not lifting. However, we recognize that the product may be utilized outside of its intended des…

FDA inspections (2)

VAI2024-08-23
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2019-07-17
Voluntary Action Indicated · Compliance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by LITTLE RAPIDS CORP.

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. “Little Rapids Corporation (FEI 1000049086) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000049086-little-rapids-corporation/

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