Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Bio-PLASTY Cannula (Needle) Recalled by Biologic Therapies, Inc Due to Devices are misbranded - failure to properly classify...

Date: January 23, 2015
Company: Biologic Therapies, Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Biologic Therapies, Inc directly.

Affected Products

Bio-PLASTY Cannula (Needle)

Quantity: 58

Why Was This Recalled?

Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution

Where Was This Sold?

This product was distributed to 7 states: CA, FL, IL, MA, NJ, TX, WA

Affected (7 states)Not affected

About Biologic Therapies, Inc

Biologic Therapies, Inc has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report