EXP Pharmaceutical Services Corp: Medical Device Recall in 2015 - (Recall #: Z-2240-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Medical Device Exchange 6.0mm Round Fluted Bur Soft Touch; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 5820-10-160; EXP (repackager), Stryker (OEM) Drills, burrs, trephines & accessories (simple, powered)

Product Classification:

Class II

Date Initiated: February 11, 2015

Date Posted: August 5, 2015

Recall Number: Z-2240-2015

Event ID: 71608

Reason for Recall:

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.

Status: Terminated

Product Quantity: 5

Code Information:

OEM Catalog number 5820-10-160.

Distribution Pattern:

Distributed in DC and the states of CO, CA, FL, TX, and AR.

Voluntary or Mandated:

Voluntary: Firm initiated