FDA Medical devices recall ·

Extended Tip Applicator, 15 CM, Box of 5 recall

This is an FDA Class I recall — the most serious type.

Recall number
Z-1959-2025
Date
(initiated May 22, 2025)
Company / brand
Integra LifeSciences Corp. (NeuroSciences)
1100 Campus Rd, Princeton, NJ, United States
Category
Medical devices › Class I
Classification
Class I
Status
Ongoing
Units affected
2,524 units
Hazard tags
Sterility
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

Product

Extended Tip Applicator, 15 CM, Box of 5.

Why was it recalled?

Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

Model/Catalog Number: 205115; UDI: 10381780000150; All Lots.

Distribution

Domestic: Nationwide Distribution; Foreign: Canada, Japan, Australia, New Zealand, Taiwan (Province of China), Mexico, Colombia, Dominican Republic (the), Singapore, Mongolia, Hong Kong, Chile, Argentina, Puerto Rico, El Salvador, Guatemala, Korea (the Republic of), Peru, Costa Rica, Panama, From Belgium, distributed to: Austria, Belgium, Cyprus, Czechia, France, Georgia, Germany, Greece, Hungary, Iran (Islamic Republic of), Ireland, Italy, Jordan, Malta, Netherlands (the), Nigeria, Palestine, State of, Portugal, Romania, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Turkey.

States: Georgia Puerto Rico

What does Class I mean?

Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.

Source: FDA (medical devices), recall Z-1959-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.