Facility

SR INSTRUMENTS, 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)	1317256
Establishment type	Manufacture Medical Device
Location	600 YOUNG ST. Tonawanda, NY, US 14150
Registration status	Active · expires 2026
Parent company	SR INSTRUMENTS, INC. (owner-operator 1317256)
Brand names	SR500, SR555; VARIOUS PATIENT STAND ON SCALE

Activity by year

Recalls (1)

Devices registered here (1)

Scale, Stand-On, Patient
Product code FRI (opens in a new tab) · Class I · General Hospital · 21 CFR 880.2700

Recalls & enforcement

Class IITerminated2012-12-13
SR Instruments Inc. is implementing a field correction for the Joerns Healthcare Patient Lifts after they received two incident reports regarding two field failures of a tensile type load cell involving the FG3105 Patient Scale. The failures resulted in patient falls.

All facilities operated by SR INSTRUMENTS, INC.

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. “SR INSTRUMENTS, INC. (FEI 1317256) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1317256-sr-instruments-inc/

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