REICHERT INC.
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
- Inspections (1)
Devices registered here (1)
- Tonometer, Ac-PoweredProduct code HKX (opens in a new tab) · Class II · Ophthalmic · 21 CFR 886.1930
Recalls & enforcement
- Class IIOngoing2025-02-28The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
- Class IIOngoing2023-07-20Phoroptor VRx Head may detach from the bracket that connects the Phoroptor VRx Head to an ophthalmic stand. If the Phoroptor VRx Head detaches from the bracket, it can fall onto a patient or device operator
FDA inspections (1)
- NAI2017-04-28No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
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.
Related
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. “REICHERT INC. (FEI 1000159913) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000159913-reichert-inc/
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