HIGHFDA DEVICE

DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst SurgicalHealth & Personal CareMedical DevicesLot Code: Model No: DVF4005-25 UDI-DI: (01)10817489021665(11)250924(17)280924(10)M50530 Lot Number: M50530 Expiration Date: 09/24/2028

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
March 25, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
March 25, 2026
Hazard Level
HIGH
Brand
Katalyst Surgical
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Katalyst Surgical
Model numbers
Lot Code: Model No: DVF4005-25 UDI-DI: (01)10817489021665(11)250924(17)280924(10)M50530 Lot Number: M50530 Expiration Date: 09/24/2028
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    March 25, 2026

  2. Reported by FDA DEVICE

    May 13, 2026

  3. RecallRadar source check

    May 20, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Katalyst Surgical, LLC or your healthcare provider for instructions. Notification method: Letter

Get instant alerts for Katalyst Surgical recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Full Description

DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25. Reason: Field Safety Corrective Action for IFU in DEX Forceps and Scissors.. Classification: Class II. Quantity: 10 units. Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

Want to Know First?

Get instant alerts for recalls that affect you. Free forever.

Product Classification

Product Details

Model Numbers
Lot Code: Model No: DVF4005-25 UDI-DI: (01)10817489021665(11)250924(17)280924(10)M50530 Lot Number: M50530 Expiration Date: 09/24/2028
Affected States
ALL
Report Date
May 13, 2026
Recall Status
ACTIVE

Related Recalls