Device recalls

Phoroptor VRx Digital Refraction System Model Numbers: 16242

Reichert, Inc. · The head of the phoropter head could come loose and potentially detach due to a default in the assembly.

Open, ClassifiedProcess controlZ-1501-2025
Open FDA's page for this record
Cfres ID
212453
Product res number
Z-1501-2025
Event date initiated
2025-02-28
Event date posted
2025-03-31
Recall status
Open, Classified
Res event number
96266
Product code
HKN
Product description
Phoroptor VRx Digital Refraction System Model Numbers: 16242
Firm FEI number
1000159913
Recalling firm
Reichert, Inc.
Address 1
3362 Walden Ave
City
Depew
State
NY
Postal code
14043-2437
Additional info contact
Richard Boerdner 716-686-4556
Reason for recall
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Root cause description
Process control
Product quantity
1876 units
Code info

Model Numbers: 16242; UDI-DI: 00812559011730; Serial Numbers: TBD; Note: The majority of units within the scope of the planned recall are older devices which do not have a UDI on the label.

Action

On February 28, 2025 "URGENT MEDICAL DEVICE RECALL" letters were sent to customers. PLEASE TAKE THE FOLLOWING ACTIONS IMMEDIATELY. 1. Inspect your Phoroptor head with reference to Figure 1 for looseness or rocking and Figure 2 for an excessive gap between components. Figure 3 shows the normal condition. 2. If your unit exhibits looseness or rocking or if there is an excessive gap between components, it is possible that your unit has the defect condition. Please remove it from service immediately and contact Reichert Technical Support at 1-888-849-8955 or at https://www.reichert.com/en/support/rma-request so that the unit can be inspected and, if necessary, repaired by Reichert. The repair will be completed at no cost to you. 3. If your unit shows the normal condition as in Figure 3, please install the Support Bracket when you receive it. It is essential that you install the Support Bracket for the safety of patients and operators even if the components appear tight and securely connected. Without the bracket, there could be eventual separation of the components. The Support Bracket prevents this possibility. The internal investigation into this issue has indicated the need for these corrections and resulted in a plan that includes actions designed to prevent a recurrence of this situation. Reichert prides itself on the quality of devices we manufacture. Please share this letter with all the relevant personnel in your organization. Please contact Reichert Technical Support with any questions. They can be reached Monday through Friday, 8:00AM to 5:00PM Eastern Time at 1-888-849-8955 or at https://www.reichert.com/en/support/support-and-service-inquiry.

Distribution pattern

Domestic: Nationwide Distribution. International: Austria, Bolivia, Canada, Denmark, France, Germany, Hong Kong, India, Israel, Italy, Morocco, Netherlands, Norway, Qatar, Saudi Arabia, Singapore, Slovakia, Switzerland, Thailand, United Arab Emirates, and United Kingdom.

Harmonized identifiers (openFDA)
Device name
Refractor, Manual, Non-Powered, Including Phoropter
Medical specialty description
Ophthalmic
Regulation number
886.1770
Device class
1
K number
K874900, K936205, K782118
Registration number
5470, 9616199, 8030392, 3008044477, 3012162565, 3014273520, 3022375836, 3038356864, 3014926240, 1000391004, 9615030, 3013403214, 3013436538, 3002894792, 3011659880, 3009515444, 2031962, 1000176188, 3010227033, 3045062165, 3006105501, 3011898560, 3009518015, 3008729548, 3003984265, 3005405896, 3009132348, 3002807715, 3007817024, 3015972897, 3009173773, 9614661, 3008197763, 3007343325, 3005771344, 3004095901, 1836161, 3010774780, 9612297, 3004784203 +24 more
FEI number
5470, 3001802794, 3008044477, 3012162565, 3014273520, 3022375836, 3038356864, 3014926240, 1000391004, 3013403214, 3002445546, 3013436538, 3002894792, 3011659880, 3009515444, 1000176188, 3001362763, 3010227033, 3045062165, 1000175127, 3006105501, 3011898560, 3009518015, 3008729548, 3003984265, 3005405896, 3009132348, 3002807715, 3007817024, 3002750084, 3009173773, 3015972897, 3008197763, 3007343325, 3005771344, 3004095901, 3010774780, 3000210228, 3004784203, 3013003882 +23 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.