Facility

HAIMEN SHENGBANG LABORATORY EQUIPMENT CO., LTD

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

Key facts

1recalls · worst Class I

—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)	3011676045
Establishment type	Manufacture Medical Device
Location	No.126,Team 9, Zhangbei Village Haimen Jiangsu, CN 22611
Registration status	Active · expires 2026
Parent company	HAIMEN SHENGBANG LABORATORY EQUIPMENT CO., LTD (owner-operator 10049185)
Brand names	face mask

Activity by year

Recalls (1)

Devices registered here (1)

Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
Product code QKR (opens in a new tab) · Not classified · Unknown

Recalls & enforcement

Class IOngoing2022-07-12
Distributed VTM outside of VTM Guidance and without clearance.

All facilities operated by HAIMEN SHENGBANG LABORATORY EQUIPMENT CO., 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. “HAIMEN SHENGBANG LABORATORY EQUIPMENT CO., LTD (FEI 3011676045) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3011676045-haimen-shengbang-laboratory-equipment-co/

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