Stryker GmbH: Medical Device Recall in 2018 - (Recall #: Z-2884-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM 1819-1220S T2 LONG PROXIMAL HUMERAL NAIL LEFT 240mm1832-2824S T2 LONG PROXIMAL HUMERAL NAIL LEFT 280mm 1832-2828S T2 LONG PROXIMAL HUMERAL NAIL RIGHT 260mm 1832-3826S T2 Ankle Arthrd Nail lft 1818-1115S

Product Classification:

Class II

Date Initiated: June 27, 2018

Date Posted: August 29, 2018

Recall Number: Z-2884-2018

Event ID: 80613

Reason for Recall:

Incomplete seal on the Tyvek lid may compromise the sterility of the device

Status: Terminated

Product Quantity: 38

Code Information:

Item Number Lot Number: 1819-1020S K0ACFED; 1819-1220S K0CAEC4; 1832-2824S K0BF6C6; 1832-2828S K0CC742; 1832-3826S K0BF6D2; 1818-1115S K0B906C

Distribution Pattern:

US distribution to KY

Voluntary or Mandated:

Voluntary: Firm initiated