Stryker GmbH recalls Stryker Locking Screw, Fully Threaded T2 Humerus ¿4x32 mm Catalog Number: 18964032S - Product Usage: Stryker implants a

Recalled June 24, 2020 · FDA recall Z-2380-2020 · Stryker

Hazard

Seal integrity of the blister pack may be compromised and sterility cannot be assured · FDA Class II

Units

OUS 40

Sold at

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, Chile, China, France, Germany, Italy, Japan, Netherlands, Poland, South Africa, Spain, Sweden, Switzerland, United Kingdom. Updated 7/21/20: Portugal, Denmark, Finland, Norway, Ireland, and Luxembourg.

Description

Seal integrity of the blister pack may be compromised and sterility cannot be assured

Product

Stryker Locking Screw, Fully Threaded T2 Humerus ¿4x32 mm Catalog Number: 18964032S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

Manufacturer(s)

Stryker GmbH

Made in

Switzerland

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →