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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 92805

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 20, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Reichert, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

PHOROPTOR VRX DIGITAL REFRACTION SYSTEM-Digital refractor intended for the subjective measurement of the refractive error of the eye. MODEL NUMBER: 16242 [Model 16241 is the base model. Model 16242 includes an additional prism feature used for the measurement of ocular deviation in patients with latent or manifest strabismus].

Z-2512-2023
Recall number
Z-2512-2023
Initiated
July 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Reichert, Inc.
Quantity
53 units; Extended 34 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Phoroptor 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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Phoroptor 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

Code information

GTIN: 0812559011730 S/N: 78824-1221 78825-1221 78826-1221 78827-1221 78828-1221 78829-1221 78830-1221 78831-1221 78832-1221 78833-1221 78834-1221 78835-1221 78836-1221 78837-1221 78838-1221 78839-1221 78840-1221 78841-1221 78842-1221 78843-1221 78844-1221 78845-1221 78846-1221 78847-1221 78848-1221 78849-1221 78850-1221 78851-1221 78852-1221 78853-0122 78854-0122 78855-0122 78856-0122 78857-0122 78858-0122 78859-0122 78860-0122 78861-0122 78862-0122 78863-0122 78864-0122 78865-0122 78866-0122 78867-0122 78868-0122 78870-0122 78871-0122 78872-0122 78873-0122 78874-0122 S/N Extended Recall 7/3/24: Serial Number 78875-0222 78876-0222 78877-0222 78878-0222 78879-0222 78880-0222 78881-0222 78882-0222 78883-0222 78884-0222 78885-0222 78886-0222 78887-0222 78888-0222 78889-0222 78890-0222 78891-0222 78892-0222 78893-0222 78894-0222 78895-0222 78896-0222 78897-0222 78898-0222 78899-0222 78900-0222 78901-0222 78902-0222 78903-0222 78904-0222 78905-0222 78906-0222 78907-0222 78908-0222 78909-0322

Distribution pattern

US Nationwide distribution.

Field note

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