Facility

Brady Worldwide

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)	3003450039
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	2221 W Camden Rd Milwaukee, WI, US 53209
Registration status	Active · expires 2026
Parent company	Precision Dynamics Corporation (owner-operator 2020282)
Brand names	Foam Cushion

Activity by year

Recalls (1)

Devices registered here (1)

Surgical Table Cushion
Product code LWG (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4950

Recalls & enforcement

Class IITerminated2013-07-10
PDC Healthcare initiated this recall of Non-Sterile Viscot Part Number 1437-100 Surgical Skin Markers, becuase they were inadvertently mislabeled as PN STER-VIS Sterile Skin Marker Pen with Labels and Flex Ruter.

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. “Brady Worldwide (FEI 3003450039) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003450039-brady-worldwide/

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