The Recall Desk
HighFDA (Devices)·Z-2252-2019·Announced 2019-08-21

BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw

BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x90 due to a manufacturing flaw in the sterile barrier system.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II. The hazard involves a sterile barrier flaw in a medical device, which poses a risk of harm (infection) even though no specific injuries or illnesses are reported in the source text.

Plain-English summary

BioPro, Inc. is recalling 4 units of the Go-EZ Screw 6.5x90, Item Number 19666. This medical device is an accessory to the BioPro Go-Ez screw system and the BioPro HBS System, intended for various orthopedic surgical procedures but not for use in the spine.

The recall was initiated due to a manufacturing flaw in the sterile barrier system. The affected units are identified by UDI M209196660, Lot Number 123113, and a manufacturing date of 4/29/2019.

The products were distributed worldwide, including in the US states of Florida, Louisiana, Maryland, North Carolina, New York, Oregon, and Texas, as well as in Ecuador and Scotland. Healthcare providers and consumers should stop using these specific units and contact BioPro, Inc. for further instructions.

The recalled product

Product
Go-EZ Screw 6.5x90, Item Number 19666 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Manufacturer
BioPro, Inc.
Affected units
4

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • UDI - M209196660 Lot Number - 123113 MFG Date - 4/29/2019

Distribution

Distributed nationwide across the United States.

The notice also names 7 states specifically:

Part of a larger recall action

This product is one of 21 recalled by BioPro, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 21 products in this recall →