Facility

WRP ASIA PACIFIC SDN. BHD.

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

Key facts

1recalls · worst Class II

1inspections · 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)	3002808507
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
Location	LOT 1, JALAN 3 SALAK TINGGI, SEPANG Selangor, MY 43900
Registration status	Active · expires 2026
Parent company	WRP ASIA PACIFIC SDN. BHD. (owner-operator 8041005)

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Latex Patient Examination Glove
Product code LYY (opens in a new tab) · Class I · General Hospital · 21 CFR 880.6250

Recalls & enforcement

Class IITerminated2018-05-07
Some left-handed gloves contain powder. Powdered surgical gloves are a banned medical device in the U.S. Powder on natural rubber latex gloves can aerosolize latex allergens, resulting in sensitization to latex and allergic reactions. Additional risks of powdered gloves include s…

FDA inspections (1)

VAI2018-09-27
Voluntary Action Indicated · Compliance: Devices

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 WRP ASIA PACIFIC SDN. BHD.

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. “WRP ASIA PACIFIC SDN. BHD. (FEI 3002808507) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002808507-wrp-asia-pacific-sdn-bhd/

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