Class II — Potential Health Hazard

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

Medical Device Exchange -SYSTEM Recalled by EXP Pharmaceutical Services Corp Due to EXP did not register as a medical device...

Date: February 11, 2015
Company: EXP Pharmaceutical Services Corp
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 EXP Pharmaceutical Services Corp directly.

Affected Products

Medical Device Exchange -SYSTEM, TACKER SKIN 5MM; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 6206; EXP (repackager), Covidien (OEM) Implantable Staple

Quantity: 3

Why Was This Recalled?

EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that its vendors were registered and had their own quality systems.

Where Was This Sold?

This product was distributed to 6 states: AR, CA, CO, FL, TX, DC

Affected (6 states)Not affected

About EXP Pharmaceutical Services Corp

EXP Pharmaceutical Services Corp has 42 total recalls tracked by RecallDetector.

Related Recalls

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