Facility

TECH GROUP GRAND RAPIDS, INC.

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)	3003595336
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	3116 N. WILSON COURT NW GR, MI, US 49534
Registration status	Active · expires 2026
Parent company	WEST PHARMACEUTICAL SERVICES, INC. (owner-operator 2514921)
Brand names	Syringe, Piston; Syringe, piston

Activity by year

Recalls (1)

Devices registered here (1)

Syringe, Piston
Product code FMF (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5860

Recalls & enforcement

Class IIOngoing2024-09-24
Due to packaging damage from heat exposure during shipping/transportation that may result in a breach in the sterile barrier.

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. “TECH GROUP GRAND RAPIDS, INC. (FEI 3003595336) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003595336-tech-group-grand-rapids-inc/

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